Chronic Systolic Heart FailureCONDI-HFNCT02248441
Effect of Remote Ischemic Conditioning in Patients With Chronic Ischemic Heart Failure
A study testing Daily ischemic conditioning treatment in people with Chronic Systolic Heart Failure, run by University of Aarhus at 1 site in Denmark.
Trial summary
The present study will evaluate whether treatment with daily remote ischemic conditioning for a 28±4-day period induces beneficial effects in subjects with and without chronic ischemic heart failure in terms of improved left ventricular contractile function and exercise capacity. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Chronic Systolic Heart Failure
- What is being tested?
- Daily ischemic conditioning treatment
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 47 participants
- Where
- 1 siteDenmark
- Study dates
- Sep 2014to Feb 2016
- 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 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- >18 years of age
- Able to understand the written patient information and to give informed consent
- Chronic congestive ischemic heart failure
- Left ventricular ejection fraction ≤45%
- New York Heart Association functional class I-III
- >18 years of age
- Able to understand the written patient information and to give informed consent
- Left ventricular ejection fraction >45%
Who cannot join
- Recent cardiovascular hospitalization (within last 30 days) • Strenuous exercise within 72 hours of either study visits
- Intake of caffeine within 24 hours of either study visit
- Intake of alcohol within 24 hours of either study visit
- Patients with permanent atrial fibrillation • Patients with diabetes mellitus
- Patients with peripheral neuropathy
- Patients in dialysis treatment
Show all 22Show fewer
- Contraindication for Magnetic Resonance Imaging examination (e.g. metal implants including Cardiac Resynchronisation Therapy devices and other pacemakers or defibrillators) precluding Magnetic Resonance Imaging
- Other concomitant disease or treatment that according to the investigator's assessment makes the patient unsuitable for study participation.
- Group 2 (Volunteers without ischemic heart disease):
- Recent cardiovascular hospitalization (within last 30 days)
- Intake of acetylsalicylic acid or non-steroidal anti-inflammatory drug medication within 7 days of either study visit
- Strenuous exercise within 72 hours of either study visit
- Intake of caffeine within 24 hours of either study visit
- Intake of alcohol within 24 hours of either study visit
- Patients with ischemic heart disease
- Patients with diabetes mellitus
- Patients with peripheral neuropathy
- Patients in dialysis treatment
- Patients in treatment with Vitamin K-antagonists, adenosine diphosphate-receptor-inhibitor, oral anticoagulants or dipyridamol.
- Conditions contraindicating short term cessation of acetylsalicylic acid and/or non-steroidal anti-inflammatory drug intake
- Contraindication for Magnetic Resonance Imaging examination (e.g. metal implants) precluding Magnetic Resonance Imaging
- Other concomitant disease or treatment that according to the investigator's assessment makes the patient unsuitable for study participation.
Trial locations and contacts
1 site in 1 country.
Denmark1 site
Aarhus University Hospital Skejby
Aarhus N, Dk-8200 Aarhus N, 8200
About this study
Official title: Effect of Remote Ischemic Conditioning in Patients With Chronic Ischemic Heart Failure (CONDI-HF)
The present study will evaluate whether treatment with daily remote ischemic conditioning for a 28±4-day period induces beneficial effects in subjects with and without chronic ischemic heart failure in terms of improved left ventricular contractile function and exercise capacity.
Read the detailed description
Background Chronic heart failure (CHF) is a leading cause of morbidity and mortality throughout the world, and the incidence and prevalence are increasing as more patients survive their acute coronary syndrome. The disease is caused by abnormalities in cardiac structure or function leading to insufficient delivery of oxygen to the metabolizing tissues. These patients are often debilitated, require chronic medications, and many receive expensive device therapy to manage symptoms. Consequently, this has led to an increasing economic and health burden from heart failure.
CHF is the end-stage of a broad range of underlying cardiovascular diseases, but is most frequently caused by ischemic heart disease. Other contributory causes include hypertension, heart valve diseases, arrhythmias and cardiomyopathies, all resulting in myocardial tissue damage and loss of ventricular function. Activation of neurohormonal and inflammatory compensatory mechanisms lead to a vicious circle through adaptive metabolic and remodeling processes, eventually resulting in a progressive decline of cardiac function with significant morbidity and mortality.
Identification of the specific underlying cardiac condition is crucial for the therapeutic approach in patients suffering from CHF. While pharmacological treatment remains dominating, resynchronization therapy and surgical resection of non-contractile tissue are also increasingly being conducted. Despite the fact that activation of the inflammatory system greatly contributes to the remodeling process through initiation of myocardial fibrosis and hypertrophy, most clinical studies targeting inflammatory components have been discouraging.
Remote ischemic conditioning (RIC) by brief non-lethal episodes of ischemia in a remote organ or tissue (e.g. a limb) is a novel therapeutic method to achieve protection against ischemia-reperfusion injury in the target organ, e.g. the heart . In the clinical setting, RIC is most often performed by repeated episodes of limb ischemia achieved by intermittent inflation of a blood pressure cuff placed around the upper arm. In clinical randomized trials, RIC has been shown to reduce the amount of myocardial injury and improve long-term outcome in patients admitted with STEMI for primary percutaneous coronary intervention and patients undergoing cardiac surgery or elective coronary intervention.
RIC is a low-cost, simple and safe procedure that can easily be conducted using a standard blood pressure cuff, and the method is increasingly used in clinical trials. The mechanisms behind RIC are not yet fully understood, but the cardioprotective effects are believed to be caused by neural and humoral signaling cascades as well as systemic anti-inflammatory effects resulting in a cytoprotective state. In addition, RIC has been shown to reduce thrombus formation. Since activation of platelets and the coagulation system are fundamental in thrombus formation and degradation, another possible mechanism of the described effects of RIC could be a result from effect on arterial thrombus formation.
The vast majority of experimental and clinical studies have utilized RIC as single-occasion treatment (i.e. 3 or 4 bouts of short limb ischemia conducted once). However, experimental studies have recently suggested that repeated RIC treatment may infer further beneficial effects. Repeated RIC application has been shown to improve endothelial function and modify leukocyte adhesion in healthy volunteers. In a rat model of myocardial infarction, RIC repeated daily for 28 days after infarction reduced adverse ventricular remodeling and improved survival. Consequently, two on-going clinical trials (clinicaltrials.gov: DREAM study NCT01664611 and CRIC-RCT study NCT01817114) are investigating the effect of repeated RIC on LVEF function in patients with reduced ventricular function after an acute coronary event. Another study investigates the effect of repeated RIC on patients with severe heart failure and left ventricular assist device (IMPULSE study NCT02044471).
So far, the effect of RIC on patients suffering from stable chronic ischemic heart failure is unknown. Furthermore, no registered studies have evaluated the effect of long-term RIC given as additive treatment to the standard medical therapy in patients with chronic ischemic heart failure.
Hypothesis
- We hypothesize, that the combination of anti-remodelling and anti-inflammatory properties together with improved endothelial function induced by repetitive RIC treatment translate into improved left ventricular function and better physical performance in subjects with CHF.
Purpose
- To determine whether RIC applied on a daily basis for 4 weeks improves left ventricular function as assessed by cardiac magnetic resonance imaging (MRI) in subjects with CHF.
- To investigate whether RIC applied on a daily basis for 4 weeks improves muscle strength, cardiopulmonary exercise capacity and thrombocyte function, and changes blood biomarker levels of inflammation and heart failure in subjects with CHF.
- To investigate whether the above-mentioned measurements differ between patients with CHF and matched subjects after RIC applied on a daily basis for 4 weeks.
Perspectives The present study will elucidate whether long-term RIC treatment induces beneficial effects in subjects with and without chronic ischemic heart failure in terms of improved left ventricular contractile function and exercise capacity, and whether long-term RIC treatment induces systemic anti-inflammatory effects in these subjects. Moreover, we find that the study can uncover some of the mechanisms behind RIC and thus potentially optimize future treatment for patients suffering, or at risk, from ischemic heart diseases.
- Conditions
- Chronic Systolic Heart Failure
- Being tested
- Daily ischemic conditioning treatment
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Daily ischemic conditioning treatmentOther
RIC stimulus will be conducted as 4 x 5 minutes upper arm ischemia achieved by inflation of a blood pressure cuff to 200 mmHg and 5 minutes reperfusion between inflations. The procedure will be performed using the AutoRICTM (CellAegis Devices Inc., Toronto, Ontario, Canada).
| Study group | Role | What they receive |
|---|---|---|
| Daily RIC | Experimental | Daily ischemic conditioning treatment Receives: Other: Daily ischemic conditioning treatment |
What is being measured
The primary outcome is the main question the study is designed to answer.
Left ventricular ejection fraction assessed by MRI
Measured: 28±4 days
Secondary outcomes (6)
Global and regional myocardial function by strain analysis assessed by MRI
Measured: 28±4 days
Left ventricular mass and end-diastolic volume assessed by MRI
Measured: 28±4 days
Cardiac output assessed by MRI
Measured: 28±4 days
Cardiopulmonary exercise capacity assessed by staged exercise bicycle test and leg extension power rig test
Measured: 28±4 days
Serology markers for heart failure
Measured: 28±4 days
Serology inflammatory markers
Measured: 28±4 days
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted25 Sep 2014 (estimated)
- Study startSep 2014
- Primary completionFeb 2016
- Study completionFeb 2016
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Chronic Systolic Heart FailureStudies of the same condition, open and under way.
- More trials run by University of AarhusThe sponsor's other registered studies.
- 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
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 47 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Aarhus
- Sponsor type
- University, hospital or other
- Collaborators
- Aarhus University Hospital Skejby, Central Jutland Regional Hospital
- Responsible party
- Sponsor
- Investigators
- Hans Erik Bøtker, Prof., Study director, Department of Cardiology, Aarhus University Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02248441
- Sponsor's protocol ID
- VEK: 1-10-72-173-14
- Acronym
- CONDI-HF
- Status last verified
- Oct 2016
- First submitted
- 2 Sep 2014
- Last updated
- 24 Aug 2017
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 24 Aug 2017. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effect of Remote Ischemic Conditioning in Patients With Chronic Ischemic Heart Failure (CONDI-HF)
- ClinicalTrials.gov ID
- NCT02248441
- Acronym / sponsor ID
- CONDI-HF / VEK: 1-10-72-173-14
- Conditions
- Chronic Systolic Heart Failure
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 47 participants (actual)
- Lead sponsor
- University of AarhusUniversity, hospital or other
- Collaborators
- Aarhus University Hospital Skejby, Central Jutland Regional Hospital
- Study start
- Sep 2014
- Primary completion
- Feb 2016 (actual)
- Study completion
- Feb 2016 (actual)
- First posted
- 25 Sep 2014 (estimated)
- 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.
The present study will evaluate whether treatment with daily remote ischemic conditioning for a 28±4-day period induces beneficial effects in subjects with and without chronic ischemic heart failure in terms of improved left ventricular contractile function and exercise capacity.
Detailed description
Background Chronic heart failure (CHF) is a leading cause of morbidity and mortality throughout the world, and the incidence and prevalence are increasing as more patients survive their acute coronary syndrome. The disease is caused by abnormalities in cardiac structure or function leading to insufficient delivery of oxygen to the metabolizing tissues. These patients are often debilitated, require chronic medications, and many receive expensive device therapy to manage symptoms. Consequently, this has led to an increasing economic and health burden from heart failure.
CHF is the end-stage of a broad range of underlying cardiovascular diseases, but is most frequently caused by ischemic heart disease. Other contributory causes include hypertension, heart valve diseases, arrhythmias and cardiomyopathies, all resulting in myocardial tissue damage and loss of ventricular function. Activation of neurohormonal and inflammatory compensatory mechanisms lead to a vicious circle through adaptive metabolic and remodeling processes, eventually resulting in a progressive decline of cardiac function with significant morbidity and mortality.
Identification of the specific underlying cardiac condition is crucial for the therapeutic approach in patients suffering from CHF. While pharmacological treatment remains dominating, resynchronization therapy and surgical resection of non-contractile tissue are also increasingly being conducted. Despite the fact that activation of the inflammatory system greatly contributes to the remodeling process through initiation of myocardial fibrosis and hypertrophy, most clinical studies targeting inflammatory components have been discouraging.
Remote ischemic conditioning (RIC) by brief non-lethal episodes of ischemia in a remote organ or tissue (e.g. a limb) is a novel therapeutic method to achieve protection against ischemia-reperfusion injury in the target organ, e.g. the heart . In the clinical setting, RIC is most often performed by repeated episodes of limb ischemia achieved by intermittent inflation of a blood pressure cuff placed around the upper arm. In clinical randomized trials, RIC has been shown to reduce the amount of myocardial injury and improve long-term outcome in patients admitted with STEMI for primary percutaneous coronary intervention and patients undergoing cardiac surgery or elective coronary intervention.
RIC is a low-cost, simple and safe procedure that can easily be conducted using a standard blood pressure cuff, and the method is increasingly used in clinical trials. The mechanisms behind RIC are not yet fully understood, but the cardioprotective effects are believed to be caused by neural and humoral signaling cascades as well as systemic anti-inflammatory effects resulting in a cytoprotective state. In addition, RIC has been shown to reduce thrombus formation. Since activation of platelets and the coagulation system are fundamental in thrombus formation and degradation, another possible mechanism of the described effects of RIC could be a result from effect on arterial thrombus formation.
The vast majority of experimental and clinical studies have utilized RIC as single-occasion treatment (i.e. 3 or 4 bouts of short limb ischemia conducted once). However, experimental studies have recently suggested that repeated RIC treatment may infer further beneficial effects. Repeated RIC application has been shown to improve endothelial function and modify leukocyte adhesion in healthy volunteers. In a rat model of myocardial infarction, RIC repeated daily for 28 days after infarction reduced adverse ventricular remodeling and improved survival. Consequently, two on-going clinical trials (clinicaltrials.gov: DREAM study NCT01664611 and CRIC-RCT study NCT01817114) are investigating the effect of repeated RIC on LVEF function in patients with reduced ventricular function after an acute coronary event. Another study investigates the effect of repeated RIC on patients with severe heart failure and left ventricular assist device (IMPULSE study NCT02044471).
So far, the effect of RIC on patients suffering from stable chronic ischemic heart failure is unknown. Furthermore, no registered studies have evaluated the effect of long-term RIC given as additive treatment to the standard medical therapy in patients with chronic ischemic heart failure.
Hypothesis
- We hypothesize, that the combination of anti-remodelling and anti-inflammatory properties together with improved endothelial function induced by repetitive RIC treatment translate into improved left ventricular function and better physical performance in subjects with CHF.
Purpose
- To determine whether RIC applied on a daily basis for 4 weeks improves left ventricular function as assessed by cardiac magnetic resonance imaging (MRI) in subjects with CHF.
- To investigate whether RIC applied on a daily basis for 4 weeks improves muscle strength, cardiopulmonary exercise capacity and thrombocyte function, and changes blood biomarker levels of inflammation and heart failure in subjects with CHF.
- To investigate whether the above-mentioned measurements differ between patients with CHF and matched subjects after RIC applied on a daily basis for 4 weeks.
Perspectives The present study will elucidate whether long-term RIC treatment induces beneficial effects in subjects with and without chronic ischemic heart failure in terms of improved left ventricular contractile function and exercise capacity, and whether long-term RIC treatment induces systemic anti-inflammatory effects in these subjects. Moreover, we find that the study can uncover some of the mechanisms behind RIC and thus potentially optimize future treatment for patients suffering, or at risk, from ischemic heart diseases.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Daily RIC | Experimental | Other: Daily ischemic conditioning treatmentDaily ischemic conditioning treatment |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (8 listed)
- >18 years of age
- Able to understand the written patient information and to give informed consent
- Chronic congestive ischemic heart failure
- Left ventricular ejection fraction ≤45%
- New York Heart Association functional class I-III
Key exclusion criteria (22 listed)
- Recent cardiovascular hospitalization (within last 30 days) • Strenuous exercise within 72 hours of either study visits
- Intake of caffeine within 24 hours of either study visit
- Intake of alcohol within 24 hours of either study visit
- Patients with permanent atrial fibrillation • Patients with diabetes mellitus
- Patients with peripheral neuropathy
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 |
|---|---|---|
| Daily ischemic conditioning treatmentRIC stimulus will be conducted as 4 x 5 minutes upper arm ischemia achieved by inflation of a blood pressure cuff to 200 mmHg and 5 minutes reperfusion between inflations. The procedure will be performed using the AutoRICTM (CellAegis Devices Inc., Toronto, Ontario, Canada). | Other | Daily RIC |
Primary outcome
Left ventricular ejection fraction assessed by MRI
Time frame: 28±4 days
6 secondary outcomes
Global and regional myocardial function by strain analysis assessed by MRI
Time frame: 28±4 days
Left ventricular mass and end-diastolic volume assessed by MRI
Time frame: 28±4 days
Cardiac output assessed by MRI
Time frame: 28±4 days
Cardiopulmonary exercise capacity assessed by staged exercise bicycle test and leg extension power rig test
Time frame: 28±4 days
Serology markers for heart failure
Time frame: 28±4 days
Serology inflammatory markers
Time frame: 28±4 days
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 24 Aug 2017.
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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.
Hans Erik Bøtker, Prof. study director
Department of Cardiology, Aarhus University Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Daily ischemic conditioning treatment in people with Chronic Systolic Heart Failure, run by University of Aarhus at 1 site in Denmark.
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 8 inclusion and 22 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 24 Aug 2017. 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 Denmark. 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. 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?
Left ventricular ejection fraction assessed by MRI (time frame: 28±4 days). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 24 Aug 2017.