Coronary Artery DiseaseEXCELNCT05913778
Long-tErm Effects of Enhanced eXternal CountErpuLsation
A study testing Enhanced external counterpulsation in people with Coronary Artery Disease and Chronic Heart Failure, run by I.M. Sechenov First Moscow State Medical University at 1 site in Russia.
Trial summary
Enhanced external counterpulsation (EECP) is an effective non-invasive treatment in patients with coronary artery disease (CAD) which complicated by chronic heart failure (CHF). Aim: to study the long-term effects of treatment with enhanced external counterpulsation on the structural and functional state of the… Read more about this study
- Who is it for?
- Ages 40 to 75 years
- Conditions the study is for
- Coronary Artery Disease, Chronic Heart Failure
- What is being tested?
- Enhanced external counterpulsation
- Type of treatment
- Medical device
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 100 participants
- Where
- 1 siteRussia
- Study dates
- 10 Dec 2020to 15 Jan 2025
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 40 to 75 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Age 40-75 years
- Verified CAD (class 2-3, stable angina) complicated by CHF (NYHA class 2-3)
- Optimal medical treatment
- Signed voluntary informed consent to participate in the study
Who cannot join
- Contraindications to treatment with EECP: recent (2-4 weeks ago) catheterization of arterial vessels; cardiac arrhythmias that can affect the synchronization of counterpulsation with the ECG; decompensated heart failure; left ventricular ejection fraction less than 30%; severe aortic insufficiency; critical ischemia of the arteries of the lower extremities; thrombosis / thrombophlebitis of the veins of the lower extremities; uncontrolled arterial hypertension (>180/110mm Hg); high pulmonary hypertension (grade 2-3; >45 mm Hg); coagulopathy, treatment with anticoagulants with prothrombin time >15 sec/INR >3; pregnancy; aneurysm of the thoracic or abdominal aorta requiring surgical treatment.
- Refusal of the patient from further participation in the study.
Trial locations and contacts
1 site in 1 country.
Russia1 site
I.M. Sechenov First Moscow State Medical University (Sechenov University)
Moscow, 119991
About this study
Official title: Long-term Effects of Enhanced External Counterpulsation on the Structural and Functional State of Blood Vessels in Patients With Coronary Heart Disease and Chronic Heart Failure
Enhanced external counterpulsation (EECP) is an effective non-invasive treatment in patients with coronary artery disease (CAD) which complicated by chronic heart failure (CHF).
Aim: to study the long-term effects of treatment with enhanced external counterpulsation on the structural and functional state of the vascular bed in patients with stable CAD complicated by CHF.
Read more
Patients (n=100) with verified stable CAD (class 2-3 angina) complicated by CHF (NYHA class 2-3) and receiving optimal drug therapy included in open randomized study.
Primary randomization (2:1) + secondary randomization (1:1).
- SHAM-counterpulsation group (ECP-SHAM; compression pressure 80 mm Hg; 35 procedures, 1 hour each);
- Active counterpulsation group (ECP35; compression pressure 220-280 mm Hg; 35 procedures, 1 hour each) 1 course per year;
- Active counterpulsation group (ECP70; compression pressure 220-280 mm Hg; 35 procedures, 1 hour each) 2 courses per year.
Duration of observation is 3 years. Stages of examination: after 3, 6, 12, 24, 36 months (after 3, 6, 12 months for the ECP-SHAM group).
Primary endpoint: combination of vascular event (myocardial infarction, acute cerebrovascular accident, revascularization procedures), hospitalization (for CAD/CHF), death.
Secondary endpoints: changes in exercise tolerance, a needing for antianginal therapy, frequency of angina episodes.
Objectives: to study the dynamics of the structural and functional state of the vascular bed (applanation tonometry, photoplethysmography, computer nailfold videocapillaroscopy), the dynamics of the clinical status (Clinical Status Assessment Scale), the dynamics of exercise tolerance (6-minute walk test), the dynamics of the quality of life of patients ( questionnaires SF36 and MLHFQ) in the ECP35 and ECP70 groups at baseline, at the end of the first course, after 6 months, 1, 2, and 3 years, and in the ECPSHAM group at baseline, at the end of the first course, after 6 and 12 months; (2) To investigate the impact of EECP on the incidence of primary (vascular events, hospitalizations for CAD/CHF, death) and secondary (frequency of angina episodes, need for antianginal drugs, exercise tolerance) endpoints.
Expected outcome of the study: Obtaining reliable data on the long-term positive effect of EECP on the dynamics of the structural and functional state of the vascular bed, exercise tolerance, quality of life and prognosis in patients with stable CAD complicated by CHF.
Read the detailed description
- Topic relevance The dominant positions of coronary artery disease (CAD) in the structure of morbidity, disability and mortality among patients with cardiovascular diseases determine the social significance of this disease. With an increase in the incidence of cardiovascular diseases from 2.483 million cases in 2000 to 4.784 million cases in 2018 (an increase of 193%), there is also an increase in newly diagnosed cases of CAD by 47%. The mortality rate from circulatory diseases in Russia over the past 15 years has decreased from 927.5 to 587.6 per 100,000 population. Achievements of modern medicine (optimization of pharmacotherapy and an increase in the number of revascularization procedures) have contributed to an improvement in the survival rates of patients with CAD. However, with an increase in life expectancy, the economic burden of atherosclerotic diseases and the need to improve the quality of life of such patients increase. Taking into account the insufficient effect of a conservative strategy in patients with severe stenoses in the coronary bed, a clear increase in the number of revascularization procedures has been observed over the past two decades. However, the limited duration of the effective functioning of stents and shunts, as well as the lack of proven benefits in terms of influencing the prognosis compared to conservative measures do not allow to fully rely on this strategy as well. In the population, there is an accumulation of the proportion of people with refractory angina pectoris, with insufficient effectiveness of the use of conservative and invasive strategies. The basis of this population is patients with progression of multivessel coronary atherosclerosis, microvascular disease, incomplete myocardial revascularization, stenosis or occlusion of shunts / stents, and patients who cannot undergo coronary bypass surgery or stenting, including repeated ones, for various other reasons. In addition, the course of coronary artery disease in such patients is often complicated by chronic heart failure (CHF), which further reduces the quality of life of patients and the prognosis. This determines the search for additional methods of treatment for these patients, which can enhance the effect of conservative and invasive strategies. Enhanced external counterpulsation (EECP) is an effective non-invasive and atraumatic treatment for patients with coronary artery disease, including complicated CHF. Preference should be given to this method in patients with severe diffuse lesions of the coronary arteries, in case of impossibility or high risk of myocardial revascularization, as well as in case of complication of heart failure. The influence of this method on the contractility of the heart, exercise tolerance and quality of life of these patients has been studied quite well. However, the long-term effects of EECP on the structural and functional state of the vascular bed (the main targets of this method) in patients with coronary artery disease complicated by CHF remain little studied.
- The novelty of the proposed topic on literary sources and patent documentation. No similarly designed studies were found in the available literature. Scientific novelty It is planned to study long-term vascular effects, the impact on exercise tolerance, quality of life, the frequency of serious adverse events, the impact on the prognosis during the treatment of EECP patients with stable CAD complicated by CHF. It is planned to expand the possible indications for EECP, optimize the treatment of EECP in patients with refractory angina and heart failure.
- Purpose and objectives of the planned research. Purpose of the study - To study the long-term effects of treatment with EECP on the structural and functional vascular state in patients with stable CAD complicated by CHF. Research objectives.
- To study the dynamics of the structural and functional vascular state (applanation tonometry, photoplethysmography, computer nailfold capillaroscopy) in active EECP groups (220-280 mm Hg; 35 procedures) 2 courses per year or 1 course per year initially, according to at the end of the course, after 6 months, 1, 2 and 3 years and in the SHAM external counterpulsation group (placebo; 80 mm Hg; 35 procedures) at baseline, at the end of the course, after 6 and 12 months;
- To study the dynamics of the clinical status (Clinical State Assessment Scale) in the groups of active EECP (220-280 mm Hg; 35 procedures) 2 courses per year or 1 course per year initially, at the end of the course, after 6 months, 1, 2 and 3 years and in the SHAM external counterpulsation group (placebo; 80 mm Hg; 35 procedures) at baseline, at the end of the course, after 6 and 12 months;
- To study the dynamics of exercise tolerance (6-minute walk test) in active EECP groups (220-280 mm Hg; 35 procedures) 2 courses per year or 1 course per year initially, at the end of the course, after 6 months, 1, 2 and 3 years and in the SHAM external counterpulsation group (placebo; 80 mm Hg; 35 procedures) at baseline, at the end of the course, after 6 and 12 months;
- To study the dynamics of the quality of life of patients (SF36 and MLHFQ questionnaires) in the groups of active EECP (220-280 mm Hg; 35 procedures) 2 courses per year or 1 course per year through the baseline, at the end of the course, 6 months, 1 , 2 and 3 years and in the SHAM external counterpulsation group (placebo; 80 mm Hg; 35 procedures) at baseline, at the end of the course, after 6 and 12 months;
- To study the dynamics of the frequency of angina pectoris episodes, the need for antianginal drugs, the frequency of vascular events, hospitalizations (for coronary artery disease / CHF), deaths in active EECP groups (220-280 mm Hg, 35 procedures) for 2 or 1 course per year and in the SHAM external counterpulsation group (placebo; 80 mm Hg; 35 procedures) during the observation period.
- To study the effect of EECP on the incidence of primary (vascular events, hospitalizations for CAD/CHF, deaths) and secondary (frequency of angina episodes, need for antianginal drugs, exercise tolerance) endpoints;
- Perform a correlation analysis between EECP treatment parameters (number of procedures and duration of treatment) with the characteristics under study (vascular and clinical effects).
- Planned type of scientific research The study is open, prospective, randomized, controlled in parallel groups.
- Object of study and the planned number of observations. The object of the study were patients (n=100) with verified CAD (class 2-3, stable angina), complicated by CHF (NYHA class 2-3), receiving optimal drug therapy.
Inclusion Criteria:
- Age 40-75 years
- Verified CAD (class 2-3, stable angina) complicated by CHF (NYHA class 2-3)
- Signed voluntary informed consent to participate in the study
Non-inclusion/exclusion criteria:
- Contraindications to treatment with EECP: recent (2-4 weeks ago) catheterization of arterial vessels; cardiac arrhythmias that can affect the synchronization of counterpulsation with the ECG; decompensated heart failure; left ventricular ejection fraction less than 30%; severe aortic insufficiency; critical ischemia of the arteries of the lower extremities; thrombosis / thrombophlebitis of the veins of the lower extremities; uncontrolled arterial hypertension (>180/110mm Hg); high pulmonary hypertension (grade 2-3; >45 mm Hg); coagulopathy, treatment with anticoagulants with prothrombin time >15 sec/INR >3; pregnancy; aneurysm of the thoracic or abdominal aorta requiring surgical treatment.
- Refusal of the patient from further participation in the study.
- Specific methods of the planned research (1) Clinical analysis of present symptoms. (2) General clinical examination, including laboratory research methods (general blood count, general urinalysis, biochemical blood test) and instrumental studies (electrocardiography, echocardiography, daily ECG monitoring, ultrasound of the vessels of the lower extremities). (3) Assessment of exercise tolerance (6-minute walk test). (4) Evaluation of the functional status (Scale for Assessment of the Clinical State as modified by V.Yu. Mareev). (5) Quality of life assessment: Questionnaire SF-36 (The Short Form-36); MLHFQ (Minnesota Living With Heart Failure Questionnaire; Minnesota Living With Heart Failure Questionnaire). (6) Non-invasive vascular examination: assessment of remodeling of the microvasculature: computer nailfold capillaroscopy (Capillaroscan-1, Russia); determination of the structural and functional state of the walls of large vessels and microvasculature: photoplethysmography (Angioscan-01, Russia); determination of the level of central arterial pressure, augmentation index: applanation tonometry (A-pulse CASPro, USA). (7) The study of patients' self-monitoring diaries (frequency of angina episodes, need for antianginal drugs), the frequency of hospitalizations for coronary artery disease/CHF, the frequency of vascular events/revascularizations.
- The expected result of the study. Obtaining reliable data on the long-term positive effect of EECP on the dynamics of the structural and functional vascular state, exercise tolerance, quality of life and prognosis in patients with stable CAD complicated by CHF. To substantiate the wider inclusion of treatment with EECP in a comprehensive program for the management of patients with CAD, including complicated CHF, along with a conservative and invasive strategy, to optimize the treatment with EECP in these patients. Presentation of the results obtained in the form of publications and implementation of the results in practical healthcare (expansion of indications for the treatment of EECP; reference to training programs for doctors).
- Base of scientific research. Department of Hospital Therapy No. 1, First Moscow State Medical University. THEM. Sechenov (University Clinical Hospital No. 1, First Moscow State Medical University named after I.M. Sechenov).
- Calendar terms of performance of work:
- Beginning of material collection December 2020
- Completion of the collection of material December 2021
- Conditions
- Coronary Artery Disease, Chronic Heart Failure
- Being tested
- Enhanced external counterpulsation
- Keywords
- coronary artery disease, chronic heart failure, enhanced external counterpulsation, structural and functional vascular state, clinical status, exercise tolerance, quality of life, cardiovascular events
- Medical subject headings
- Coronary Artery Disease
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Enhanced external counterpulsationDevice
Also called EECP
Enhanced external counterpulsation (EECP) is a noninvasive therapy for the treatment of patients with coronary artery disease.The systolic deflation/diastolic inflation sequence of EECP leads to systolic unloading and diastolic augmentation, resulting in increased blood flow in a pulsatile manner in coronary artery and in others organ arteries.
| Study group | Role | What they receive |
|---|---|---|
| Enhanced external counterpulsation 35 hours per year | Experimental | Subjects with Heart failure with Enhanced external counterpulsation therapy (inflation pressure 220-280 mm Hg; 35 procedures) was given as a 1-hour session, once daily, for a total of 35 sessions, 1 course per 12 months Receives: Device: Enhanced external counterpulsation |
| Enhanced external counterpulsation 70 hours per year | Experimental | Subjects with Heart failure with Enhanced external counterpulsation therapy (inflation pressure 220-280 mm Hg; 35 procedures) was given as a 1-hour session, once daily, for a total of 35 sessions, 1 course per 6 months Receives: Device: Enhanced external counterpulsation |
| SHAM external counterpulsation | Sham comparator | Subjects with Heart failure with SHAM external counterpulsation (inflation pressure 80 mm Hg; 35 procedures) was given as a 1-hour session, once daily, for a total of 35 sessions, 1 course per 12 months Receives: Device: Enhanced external counterpulsation |
What is being measured
The primary outcome is the main question the study is designed to answer.
Composite primary endpoint
combination of vascular event (myocardial infarction, acute cerebrovascular accident, revascularization procedures), hospitalization (for CAD/CHF), death
Measured: 12 months, 24 months, 36 months
Secondary outcomes (3)
Exercise tolerance
changes in exercise tolerance (6-minute walk test)
Measured: 3 months, 6 months, 12 months, 24 months, 36 months
Antianginal therapy
changes in need for antianginal therapy (nitroglycerin doses per week)
Measured: 12 months, 24 months, 36 months
Angina episodes
changes in frequency of angina episodes
Measured: 12 months, 24 months, 36 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Jun 2023
- Study start10 Dec 2020
- Primary completion10 Dec 2021
- Study completion15 Jan 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (13)Papers the sponsor has linked to this study.
- Other trials for Coronary Artery DiseaseStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- open, prospective, randomized, controlled in parallel groups
- Masking
- None (open label)
- Enrolment
- 100 participants (actual)
Sponsor and investigators
- Lead sponsor
- I.M. Sechenov First Moscow State Medical University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Alexey Lishuta, MD, PhD, Principal investigator, I.M. Sechenov First Moscow State Medical University (Sechenov University)
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05913778
- Sponsor's protocol ID
- SUCT10122020
- Acronym
- EXCEL
- Status last verified
- Oct 2024
- First submitted
- 1 Jun 2023
- Last updated
- 9 Apr 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Publications
Karaganov K.S., Lishuta A.S., Belenkov Y.N. The Use of Enhanced External Counterpulsation in the Treatment of Patients with Coronary Artery Disease. Rational Pharmacotherapy in Cardiology. 2020;16(4):579-584. (In Russ.) https://doi.org/10.20996/1819-6446-2020-08-07
Karaganov K.S., Slepova O.A., Lishuta A.S., Solomakhina N.I., Belenkov Yu.N. Medium-term Effects of Enhanced External Counterpulsation in the Structural and Functional Parameters of Blood Vessels in Patients with Coronary Artery Disease. Rational Pharmacotherapy in Cardiology. 2021;17(4):557-563. https://doi.org/10.20996/1819-6446-2021-08-03
Slepova O.A., Lishuta A.S., Vasiltsova E.Yu., Privalova E.V., Belenkov Yu.N. The Effect of Enhanced External Counterpulsation on the Vascular State, Indicators of Glycemic Control and Quality of Life in Patients with Coronary Artery Disease and Type 2 Diabetes Mellitus. Rational Pharmacotherapy in Cardiology. 2022;18(3):274-281. https://doi.org/10.20996/1819-6446-2022-06-04
Mamieva Z.A., Lishuta A.S., Belenkov Yu.N., Privalova E.V., Yusupova A.O., Rykova S.M. POSSIBILITIES OF ENHANCED EXTERNAL COUNTERPULSATION USING IN CLINICAL PRACTICE. Rational Pharmacotherapy in Cardiology. 2017;13(2):238-247. (In Russ.) https://doi.org/10.20996/1819-6446-2017-13-2-238-247
Lishuta A.S., Nikolaeva N.A., Belenkov Yu.N. Long-term vascular effects of enhanced external counterpulsation in patients with coronary artery disease complicated by heart failure. Medical and pharmaceutical journal "Pulse". 2024; 26 (4): 81-89. http://dx.doi.org//10.26787/nydha-2686-6838-2024-26-4-81-89
Lishuta A.S., Slepova O.A., Nikolaeva N.A., Belenkov Yu.N. Medium-term effects of enhanced external counterpulsation on markers of glycemic control in patients with chronic heart failure of ischemic genesis. Medical and pharmaceutical journal "Pulse". 2024; 26 (5): 92-99. http://dx.doi.org//10.26787/nydha-2686-6838-2024-26-5-92-99
Lishuta A.S., Nikolaeva N.A., Belenkov Yu.N. Long-term effectiveness of enhanced external counterpulsation in patients with chronic heart failure of ischemic genesis. Medical and pharmaceutical journal "Pulse". 2024; 26 (6): 63-70. http://dx.doi.org//10.26787/nydha-2686-6838-2024-26-6-63-70
Lishuta A.S., Slepova O.A., Nikolaeva N.A., Privalova E.V., Belenkov Yu.N. Long-term effects of enhanced external counterpulsation in the management of patients with coronary artery disease complicated by heart failure: data from the EXCEL study. Creative cardiology. 2024; 18 (2): 194-201. DOI: 10.24022/1997-3187-2024-18-2-194-201
Belenkov YN, Lishuta AS, Slepova OA, Nikolaeva NS, Khabarova NV, Dadashova GM, Privalova EV. The EXCEL Study: Long-term Observation of the Effectiveness of Drug and Non-drug Rehabilitation in Patients with Ischemic Heart Failure. Kardiologiia. 2024 Jan 31;64(1):14-24. doi: 10.18087/cardio.2024.1.n2615. English, Russian.
PubMed 38323440Lishuta A.S., Slepova O.A., Nikolaeva N.A., Khabarova N.V., Privalova E.V., Belenkov Yu.N. Effectiveness of different treatment regimens of enhanced external counterpulsation in patients with stable coronary artery disease complicated by heart failure. Rational Pharmacotherapy in Cardiology. 2024;20(1):35-45. https://doi.org/10.20996/1819-6446-2024-3004.
Lishuta A.S., Slepova O.A., Nikolaeva N.A., Petruhnova M.F., Privalova E.V., Belenkov Yu.N. Long-term effects of enhanced external counterpulsation in the management of patients with ischemic chronic heart failure. Rational Pharmacotherapy in Cardiology. 2024;20(2):194-201. https://doi.org/10.20996/1819-6446-2024-3041
Lishuta A.S., Slepova O.A., Nikolaeva N.S., Privalova E.V., Belenkov Yu.N. Long-term effects of enhanced external counterpulsation in the management of patients with coronary artery disease complicated by heart failure: data from the EXCEL study. Russian Journal of Cardiology. 2024;29(6):5886. https://doi.org/10.15829/1560-4071-20245886.
Lishuta A.S., Privalova E.V., Belenkov Yu.N. Enhanced external counterpulsation in the management of patients with ischemic heart failure: long-term impact on clinical outcomes. Cardiovascular Therapy and Prevention. 024;23(8):4015. https://doi.org/10.15829/1728-88002024-4015
Study at a glance
From the registry record, last updated by the sponsor on 9 Apr 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Long-term Effects of Enhanced External Counterpulsation on the Structural and Functional State of Blood Vessels in Patients With Coronary Heart Disease and Chronic Heart Failure
- ClinicalTrials.gov ID
- NCT05913778
- Acronym / sponsor ID
- EXCEL / SUCT10122020
- Conditions
- Coronary Artery Disease, Chronic Heart Failure
- Keywords
- coronary artery disease, chronic heart failure, enhanced external counterpulsation, structural and functional vascular state, clinical status, exercise tolerance, quality of life, cardiovascular events
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 100 participants (actual)
- Lead sponsor
- I.M. Sechenov First Moscow State Medical UniversityUniversity, hospital or other
- Study start
- 10 Dec 2020 (actual)
- Primary completion
- 10 Dec 2021 (actual)
- Study completion
- 15 Jan 2025 (actual)
- First posted
- 22 Jun 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Enhanced external counterpulsation (EECP) is an effective non-invasive treatment in patients with coronary artery disease (CAD) which complicated by chronic heart failure (CHF).
Aim: to study the long-term effects of treatment with enhanced external counterpulsation on the structural and functional state of the vascular bed in patients with stable CAD complicated by CHF.
Patients (n=100) with verified stable CAD (class 2-3 angina) complicated by CHF (NYHA class 2-3) and receiving optimal drug therapy included in open randomized study.
Primary randomization (2:1) + secondary randomization (1:1).
- SHAM-counterpulsation group (ECP-SHAM; compression pressure 80 mm Hg; 35 procedures, 1 hour each);
- Active counterpulsation group (ECP35; compression pressure 220-280 mm Hg; 35 procedures, 1 hour each) 1 course per year;
- Active counterpulsation group (ECP70; compression pressure 220-280 mm Hg; 35 procedures, 1 hour each) 2 courses per year.
Duration of observation is 3 years. Stages of examination: after 3, 6, 12, 24, 36 months (after 3, 6, 12 months for the ECP-SHAM group).
Primary endpoint: combination of vascular event (myocardial infarction, acute cerebrovascular accident, revascularization procedures), hospitalization (for CAD/CHF), death.
Secondary endpoints: changes in exercise tolerance, a needing for antianginal therapy, frequency of angina episodes.
Objectives: to study the dynamics of the structural and functional state of the vascular bed (applanation tonometry, photoplethysmography, computer nailfold videocapillaroscopy), the dynamics of the clinical status (Clinical Status Assessment Scale), the dynamics of exercise tolerance (6-minute walk test), the dynamics of the quality of life of patients ( questionnaires SF36 and MLHFQ) in the ECP35 and ECP70 groups at baseline, at the end of the first course, after 6 months, 1, 2, and 3 years, and in the ECPSHAM group at baseline, at the end of the first course, after 6 and 12 months; (2) To investigate the impact of EECP on the incidence of primary (vascular events, hospitalizations for CAD/CHF, death) and secondary (frequency of angina episodes, need for antianginal drugs, exercise tolerance) endpoints.
Expected outcome of the study: Obtaining reliable data on the long-term positive effect of EECP on the dynamics of the structural and functional state of the vascular bed, exercise tolerance, quality of life and prognosis in patients with stable CAD complicated by CHF.
Detailed description
- Topic relevance The dominant positions of coronary artery disease (CAD) in the structure of morbidity, disability and mortality among patients with cardiovascular diseases determine the social significance of this disease. With an increase in the incidence of cardiovascular diseases from 2.483 million cases in 2000 to 4.784 million cases in 2018 (an increase of 193%), there is also an increase in newly diagnosed cases of CAD by 47%. The mortality rate from circulatory diseases in Russia over the past 15 years has decreased from 927.5 to 587.6 per 100,000 population. Achievements of modern medicine (optimization of pharmacotherapy and an increase in the number of revascularization procedures) have contributed to an improvement in the survival rates of patients with CAD. However, with an increase in life expectancy, the economic burden of atherosclerotic diseases and the need to improve the quality of life of such patients increase. Taking into account the insufficient effect of a conservative strategy in patients with severe stenoses in the coronary bed, a clear increase in the number of revascularization procedures has been observed over the past two decades. However, the limited duration of the effective functioning of stents and shunts, as well as the lack of proven benefits in terms of influencing the prognosis compared to conservative measures do not allow to fully rely on this strategy as well. In the population, there is an accumulation of the proportion of people with refractory angina pectoris, with insufficient effectiveness of the use of conservative and invasive strategies. The basis of this population is patients with progression of multivessel coronary atherosclerosis, microvascular disease, incomplete myocardial revascularization, stenosis or occlusion of shunts / stents, and patients who cannot undergo coronary bypass surgery or stenting, including repeated ones, for various other reasons. In addition, the course of coronary artery disease in such patients is often complicated by chronic heart failure (CHF), which further reduces the quality of life of patients and the prognosis. This determines the search for additional methods of treatment for these patients, which can enhance the effect of conservative and invasive strategies. Enhanced external counterpulsation (EECP) is an effective non-invasive and atraumatic treatment for patients with coronary artery disease, including complicated CHF. Preference should be given to this method in patients with severe diffuse lesions of the coronary arteries, in case of impossibility or high risk of myocardial revascularization, as well as in case of complication of heart failure. The influence of this method on the contractility of the heart, exercise tolerance and quality of life of these patients has been studied quite well. However, the long-term effects of EECP on the structural and functional state of the vascular bed (the main targets of this method) in patients with coronary artery disease complicated by CHF remain little studied.
- The novelty of the proposed topic on literary sources and patent documentation. No similarly designed studies were found in the available literature. Scientific novelty It is planned to study long-term vascular effects, the impact on exercise tolerance, quality of life, the frequency of serious adverse events, the impact on the prognosis during the treatment of EECP patients with stable CAD complicated by CHF. It is planned to expand the possible indications for EECP, optimize the treatment of EECP in patients with refractory angina and heart failure.
- Purpose and objectives of the planned research. Purpose of the study - To study the long-term effects of treatment with EECP on the structural and functional vascular state in patients with stable CAD complicated by CHF. Research objectives.
- To study the dynamics of the structural and functional vascular state (applanation tonometry, photoplethysmography, computer nailfold capillaroscopy) in active EECP groups (220-280 mm Hg; 35 procedures) 2 courses per year or 1 course per year initially, according to at the end of the course, after 6 months, 1, 2 and 3 years and in the SHAM external counterpulsation group (placebo; 80 mm Hg; 35 procedures) at baseline, at the end of the course, after 6 and 12 months;
- To study the dynamics of the clinical status (Clinical State Assessment Scale) in the groups of active EECP (220-280 mm Hg; 35 procedures) 2 courses per year or 1 course per year initially, at the end of the course, after 6 months, 1, 2 and 3 years and in the SHAM external counterpulsation group (placebo; 80 mm Hg; 35 procedures) at baseline, at the end of the course, after 6 and 12 months;
- To study the dynamics of exercise tolerance (6-minute walk test) in active EECP groups (220-280 mm Hg; 35 procedures) 2 courses per year or 1 course per year initially, at the end of the course, after 6 months, 1, 2 and 3 years and in the SHAM external counterpulsation group (placebo; 80 mm Hg; 35 procedures) at baseline, at the end of the course, after 6 and 12 months;
- To study the dynamics of the quality of life of patients (SF36 and MLHFQ questionnaires) in the groups of active EECP (220-280 mm Hg; 35 procedures) 2 courses per year or 1 course per year through the baseline, at the end of the course, 6 months, 1 , 2 and 3 years and in the SHAM external counterpulsation group (placebo; 80 mm Hg; 35 procedures) at baseline, at the end of the course, after 6 and 12 months;
- To study the dynamics of the frequency of angina pectoris episodes, the need for antianginal drugs, the frequency of vascular events, hospitalizations (for coronary artery disease / CHF), deaths in active EECP groups (220-280 mm Hg, 35 procedures) for 2 or 1 course per year and in the SHAM external counterpulsation group (placebo; 80 mm Hg; 35 procedures) during the observation period.
- To study the effect of EECP on the incidence of primary (vascular events, hospitalizations for CAD/CHF, deaths) and secondary (frequency of angina episodes, need for antianginal drugs, exercise tolerance) endpoints;
- Perform a correlation analysis between EECP treatment parameters (number of procedures and duration of treatment) with the characteristics under study (vascular and clinical effects).
- Planned type of scientific research The study is open, prospective, randomized, controlled in parallel groups.
- Object of study and the planned number of observations. The object of the study were patients (n=100) with verified CAD (class 2-3, stable angina), complicated by CHF (NYHA class 2-3), receiving optimal drug therapy.
Inclusion Criteria:
- Age 40-75 years
- Verified CAD (class 2-3, stable angina) complicated by CHF (NYHA class 2-3)
- Signed voluntary informed consent to participate in the study
Non-inclusion/exclusion criteria:
- Contraindications to treatment with EECP: recent (2-4 weeks ago) catheterization of arterial vessels; cardiac arrhythmias that can affect the synchronization of counterpulsation with the ECG; decompensated heart failure; left ventricular ejection fraction less than 30%; severe aortic insufficiency; critical ischemia of the arteries of the lower extremities; thrombosis / thrombophlebitis of the veins of the lower extremities; uncontrolled arterial hypertension (>180/110mm Hg); high pulmonary hypertension (grade 2-3; >45 mm Hg); coagulopathy, treatment with anticoagulants with prothrombin time >15 sec/INR >3; pregnancy; aneurysm of the thoracic or abdominal aorta requiring surgical treatment.
- Refusal of the patient from further participation in the study.
- Specific methods of the planned research (1) Clinical analysis of present symptoms. (2) General clinical examination, including laboratory research methods (general blood count, general urinalysis, biochemical blood test) and instrumental studies (electrocardiography, echocardiography, daily ECG monitoring, ultrasound of the vessels of the lower extremities). (3) Assessment of exercise tolerance (6-minute walk test). (4) Evaluation of the functional status (Scale for Assessment of the Clinical State as modified by V.Yu. Mareev). (5) Quality of life assessment: Questionnaire SF-36 (The Short Form-36); MLHFQ (Minnesota Living With Heart Failure Questionnaire; Minnesota Living With Heart Failure Questionnaire). (6) Non-invasive vascular examination: assessment of remodeling of the microvasculature: computer nailfold capillaroscopy (Capillaroscan-1, Russia); determination of the structural and functional state of the walls of large vessels and microvasculature: photoplethysmography (Angioscan-01, Russia); determination of the level of central arterial pressure, augmentation index: applanation tonometry (A-pulse CASPro, USA). (7) The study of patients' self-monitoring diaries (frequency of angina episodes, need for antianginal drugs), the frequency of hospitalizations for coronary artery disease/CHF, the frequency of vascular events/revascularizations.
- The expected result of the study. Obtaining reliable data on the long-term positive effect of EECP on the dynamics of the structural and functional vascular state, exercise tolerance, quality of life and prognosis in patients with stable CAD complicated by CHF. To substantiate the wider inclusion of treatment with EECP in a comprehensive program for the management of patients with CAD, including complicated CHF, along with a conservative and invasive strategy, to optimize the treatment with EECP in these patients. Presentation of the results obtained in the form of publications and implementation of the results in practical healthcare (expansion of indications for the treatment of EECP; reference to training programs for doctors).
- Base of scientific research. Department of Hospital Therapy No. 1, First Moscow State Medical University. THEM. Sechenov (University Clinical Hospital No. 1, First Moscow State Medical University named after I.M. Sechenov).
- Calendar terms of performance of work:
- Beginning of material collection December 2020
- Completion of the collection of material December 2021
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 3
- Model description
- open, prospective, randomized, controlled in parallel groups
| Arm | Type | Receives |
|---|---|---|
| Enhanced external counterpulsation 35 hours per year | Experimental | Device: Enhanced external counterpulsationSubjects with Heart failure with Enhanced external counterpulsation therapy (inflation pressure 220-280 mm Hg; 35 procedures) was given as a 1-hour session, once daily, for a total of 35 sessions, 1 course per 12 months |
| Enhanced external counterpulsation 70 hours per year | Experimental | Device: Enhanced external counterpulsationSubjects with Heart failure with Enhanced external counterpulsation therapy (inflation pressure 220-280 mm Hg; 35 procedures) was given as a 1-hour session, once daily, for a total of 35 sessions, 1 course per 6 months |
| SHAM external counterpulsation | Sham comparator | Device: Enhanced external counterpulsationSubjects with Heart failure with SHAM external counterpulsation (inflation pressure 80 mm Hg; 35 procedures) was given as a 1-hour session, once daily, for a total of 35 sessions, 1 course per 12 months |
Who may qualify
- Ages
- 40 to 75 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Age 40-75 years
- Verified CAD (class 2-3, stable angina) complicated by CHF (NYHA class 2-3)
- Optimal medical treatment
- Signed voluntary informed consent to participate in the study
Key exclusion criteria (2 listed)
- Contraindications to treatment with EECP: recent (2-4 weeks ago) catheterization of arterial vessels; cardiac arrhythmias that can affect the synchronization of counterpulsation with the ECG; decompensated heart failure; left ventricular ejection fraction less than 30%; severe aortic insufficiency; critical ischemia of the arteries of the lower extremities; thrombosis / thrombophlebitis of the veins of the lower extremities; uncontrolled arterial hypertension (>180/110mm Hg); high pulmonary hypertension (grade 2-3; >45 mm Hg); coagulopathy, treatment with anticoagulants with prothrombin time >15 sec/INR >3; pregnancy; aneurysm of the thoracic or abdominal aorta requiring surgical treatment.
- Refusal of the patient from further participation in the study.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Enhanced external counterpulsationAlso: EECPEnhanced external counterpulsation (EECP) is a noninvasive therapy for the treatment of patients with coronary artery disease.The systolic deflation/diastolic inflation sequence of EECP leads to systolic unloading and diastolic augmentation, resulting in increased blood flow in a pulsatile manner in coronary artery and in others organ arteries. | Device | Enhanced external counterpulsation 35 hours per year, Enhanced external counterpulsation 70 hours per year, SHAM external counterpulsation |
Primary outcome
Composite primary endpoint
Time frame: 12 months, 24 months, 36 months
combination of vascular event (myocardial infarction, acute cerebrovascular accident, revascularization procedures), hospitalization (for CAD/CHF), death
3 secondary outcomes
Exercise tolerance
Time frame: 3 months, 6 months, 12 months, 24 months, 36 months
Antianginal therapy
Time frame: 12 months, 24 months, 36 months
Angina episodes
Time frame: 12 months, 24 months, 36 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 9 Apr 2025.
- BackgroundKaraganov K.S., Lishuta A.S., Belenkov Y.N. The Use of Enhanced External Counterpulsation in the Treatment of Patients with Coronary Artery Disease. Rational Pharmacotherapy in Cardiology. 2020;16(4):579-584. (In Russ.) https://doi.org/10.20996/1819-6446-2020-08-07
- BackgroundKaraganov K.S., Slepova O.A., Lishuta A.S., Solomakhina N.I., Belenkov Yu.N. Medium-term Effects of Enhanced External Counterpulsation in the Structural and Functional Parameters of Blood Vessels in Patients with Coronary Artery Disease. Rational Pharmacotherapy in Cardiology. 2021;17(4):557-563. https://doi.org/10.20996/1819-6446-2021-08-03
- BackgroundSlepova O.A., Lishuta A.S., Vasiltsova E.Yu., Privalova E.V., Belenkov Yu.N. The Effect of Enhanced External Counterpulsation on the Vascular State, Indicators of Glycemic Control and Quality of Life in Patients with Coronary Artery Disease and Type 2 Diabetes Mellitus. Rational Pharmacotherapy in Cardiology. 2022;18(3):274-281. https://doi.org/10.20996/1819-6446-2022-06-04
- BackgroundMamieva Z.A., Lishuta A.S., Belenkov Yu.N., Privalova E.V., Yusupova A.O., Rykova S.M. POSSIBILITIES OF ENHANCED EXTERNAL COUNTERPULSATION USING IN CLINICAL PRACTICE. Rational Pharmacotherapy in Cardiology. 2017;13(2):238-247. (In Russ.) https://doi.org/10.20996/1819-6446-2017-13-2-238-247
- Results publicationLishuta A.S., Nikolaeva N.A., Belenkov Yu.N. Long-term vascular effects of enhanced external counterpulsation in patients with coronary artery disease complicated by heart failure. Medical and pharmaceutical journal "Pulse". 2024; 26 (4): 81-89. http://dx.doi.org//10.26787/nydha-2686-6838-2024-26-4-81-89
- Results publicationLishuta A.S., Slepova O.A., Nikolaeva N.A., Belenkov Yu.N. Medium-term effects of enhanced external counterpulsation on markers of glycemic control in patients with chronic heart failure of ischemic genesis. Medical and pharmaceutical journal "Pulse". 2024; 26 (5): 92-99. http://dx.doi.org//10.26787/nydha-2686-6838-2024-26-5-92-99
- Results publicationLishuta A.S., Nikolaeva N.A., Belenkov Yu.N. Long-term effectiveness of enhanced external counterpulsation in patients with chronic heart failure of ischemic genesis. Medical and pharmaceutical journal "Pulse". 2024; 26 (6): 63-70. http://dx.doi.org//10.26787/nydha-2686-6838-2024-26-6-63-70
- Results publicationLishuta A.S., Slepova O.A., Nikolaeva N.A., Privalova E.V., Belenkov Yu.N. Long-term effects of enhanced external counterpulsation in the management of patients with coronary artery disease complicated by heart failure: data from the EXCEL study. Creative cardiology. 2024; 18 (2): 194-201. DOI: 10.24022/1997-3187-2024-18-2-194-201
- Results publication: PubMed 38323440Belenkov YN, Lishuta AS, Slepova OA, Nikolaeva NS, Khabarova NV, Dadashova GM, Privalova EV. The EXCEL Study: Long-term Observation of the Effectiveness of Drug and Non-drug Rehabilitation in Patients with Ischemic Heart Failure. Kardiologiia. 2024 Jan 31;64(1):14-24. doi: 10.18087/cardio.2024.1.n2615. English, Russian.
- Results publicationLishuta A.S., Slepova O.A., Nikolaeva N.A., Khabarova N.V., Privalova E.V., Belenkov Yu.N. Effectiveness of different treatment regimens of enhanced external counterpulsation in patients with stable coronary artery disease complicated by heart failure. Rational Pharmacotherapy in Cardiology. 2024;20(1):35-45. https://doi.org/10.20996/1819-6446-2024-3004.
- Results publicationLishuta A.S., Slepova O.A., Nikolaeva N.A., Petruhnova M.F., Privalova E.V., Belenkov Yu.N. Long-term effects of enhanced external counterpulsation in the management of patients with ischemic chronic heart failure. Rational Pharmacotherapy in Cardiology. 2024;20(2):194-201. https://doi.org/10.20996/1819-6446-2024-3041
- Results publicationLishuta A.S., Slepova O.A., Nikolaeva N.S., Privalova E.V., Belenkov Yu.N. Long-term effects of enhanced external counterpulsation in the management of patients with coronary artery disease complicated by heart failure: data from the EXCEL study. Russian Journal of Cardiology. 2024;29(6):5886. https://doi.org/10.15829/1560-4071-20245886.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Alexey Lishuta, MD, PhD principal investigator
I.M. Sechenov First Moscow State Medical University (Sechenov University)
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Enhanced external counterpulsation in people with Coronary Artery Disease and Chronic Heart Failure, run by I.M. Sechenov First Moscow State Medical University at 1 site in Russia.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 9 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Russia. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Composite primary endpoint (time frame: 12 months, 24 months, 36 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05913778, which also lists 13 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Apr 2025.