HypertensionEECPNCT00953797
Role of Enhanced External Counterpulsation (EECP) Therapy in Patients With Resistant Hypertension
A study testing Enhanced External Counterpulsation in people with Hypertension, run by Albert Einstein Healthcare Network at 1 site in United States.
Trial summary
High Blood Pressure or Hypertension is one of the main causes of stroke, heart disease, heart attack and kidney disease. Traditionally physicians use diet and lifestyles change and medications to control patient's blood pressure. Read more about this study
- Who is it for?
- Ages 18 to 80 years
- Conditions the study is for
- Hypertension
- What is being tested?
- Enhanced External Counterpulsation
- Type of treatment
- Medical device
- How many people
- 0 participants
- Where
- 1 siteUnited States
- Study dates
- May 2009to Oct 2011
- 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 to 80 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Subjects who are competent to provide written consent
- Aged 18 to 80 years
- Deemed to be compliant with anti-hypertension medication therapy.
- Subjects with diabetes and/or chronic kidney disease must have a mean systolic blood pressure ≥130 mmHg
- All other subjects must have a mean systolic blood pressure ≥140 mmHg
- Receiving and adhering to full doses of appropriate guideline-recommended antihypertensive drugs from three different classes of antihypertensive agents, including a diuretic
- Female subjects of non-childbearing potential (i.e., post-menopausal for at least 2 years; surgically sterile)
- Deemed to be compliant with anti-hypertension medication therapy
Who cannot join
- Average sitting systolic blood pressure ≥180 mmHg or diastolic blood pressure ≥110 mmHg
- Known Sleep apnea
- Subjects who have participated in a clinical study involving another investigational drug or device within 4 weeks prior to Screening
- Have hypertension secondary to an identifiable and treatable cause other than sleep apnea
- Acute coronary syndrome < 6 weeks prior to enrollment
- Non-bypassable left main coronary with a luminal stenosis ≥ 50%
Show all 25Show fewer
- CABG < 3 months or PCI < 6 months prior to enrollment
- Cardiac catheterization < 2 weeks prior to enrollment
- Arrhythmias that would significantly interfere with the triggering of the EECP device.
- Clinically significant valvular heart disease
- Acute myocarditis
- ICD if it has been triggered < 3 months prior to enrollment
- History of deep vein thrombosis, phlebitis, stasis ulcer, pulmonary embolism, and/or aortic aneurysm
- INR ≥ 2.5
- Patients taking over the counter medications that can raise blood pressure, such as
- Non narcotic analgesics
- Non steroidal anti-inflammatory agents, including aspirin, Selective COX-2 inhibitors
- Sympathomimetic agents (decongestants, diet pills, cocaine)
- Stimulants (methylphenidate, dexmethylphenidate, dextroamphetamine, amphetamine, methamphetamine, modafinil)
- Alcohol
- Oral contraceptives
- Cyclosporine
- Erythropoietin
- Natural licorice
- Herbal compounds (ephedra or ma huang)
Trial locations and contacts
1 site in 1 country.
United States1 site
Albert Einstein Medical Center
Philadelphia, Pennsylvania, 19141
About this study
Official title: Role of EECP Therapy in Patients With Resistant Hypertension
High Blood Pressure or Hypertension is one of the main causes of stroke, heart disease, heart attack and kidney disease. Traditionally physicians use diet and lifestyles change and medications to control patient's blood pressure. There are however, some patients whose blood pressures are difficult to control and their blood pressure remains elevated despite multiple medications. When blood pressure remains above goal (greater then 140/90 or greater then 130/80 mmHg in patients with diabetes or kidney disease) despite 3 or more blood pressure medications, the investigators call it "Resistant Hypertension".
Enhanced External Counterpulsation (EECP) is a new method of treatment currently used in people with heart disease and chest pain. EECP therapy uses three sets of balloon like cuffs that are wrapped to the calves, lower thighs, and upper thighs. These cuffs inflate and deflate with every heart beat, causing increased blood return to the heart and better blood flow. It has also been found to improve the function of endothelial cells, a type of cells that lines the wall of blood vessel through out the body which helps to regulate and maintain blood pressure. This leads us to believe that EECP therapy, although not used at present for treating patients with Resistant Hypertension, may be useful in decreasing blood pressure.
Read the detailed description
Hypertension is a major cause and contributor to stroke, heart and kidney disease and could worsen the progression as well. Despite major reductions in age-adjusted death rates from coronary heart disease and stroke, these continue to be the leading and third most common causes of death, respectively, in the United States. In particular, for every 20 mm Hg increase in systolic blood pressure or 10 mm Hg in diastolic blood pressure, there is a doubling of stroke and coronary artery disease death rates. Kidney Failure related to hypertension continues to grow, especially among the African-American population.
Traditional approaches have mostly included pharmaceuticals targeting different mechanisms that contribute to HTN. However, adequate control of Blood pressure continues to remain a major problem.
Resistant hypertension is defined as blood pressure that remains above goal in spite of the concurrent use of three antihypertensive agents of different classes. Ideally, one of the three agents should be a diuretic and all agents should be prescribed at optimal dose amounts. Patients whose blood pressure is controlled but require four or more medications to do so should be considered resistant to treatment. The prevalence of resistant hypertension is unknown. Cross- sectional studies and hypertension outcome studies suggest, however, that it is not uncommon. In a recent analysis of National Health and Nutrition Examination Survey (NHANES) participants being treated for hypertension, only 53% were controlled to <140/90 mm Hg. In a cross-sectional analysis of Framingham Heart Study participants, only 48% of treated participants were controlled to <140/90 mm Hg and less than 40% of elderly participants (>75 years of age) were at a goal blood pressure.
The benefits of successful treatment, however, are likely substantial as suggested by hypertension outcome studies in general and by the early Veterans Administration cooperative studies, which demonstrated a 96% reduction in cardiovascular events over 18 months with use of triple antihypertensive regimens compared with placebo in patients with severe hypertension (diastolic blood pressure 115 to 129 mm Hg).
Furthermore, as age and obesity are the two most common risk factors for hypertension the prevalence will likely increase as the patient population gets older and heavier. This necessitates development of novel therapeutic approaches to blood pressure control.
Enhanced External Counterpulsation (EECP) is a non-invasive method currently used for the treatment of ischemic coronary disease. During EECP therapy three compressive pneumatic cuffs are wrapped to the calves, lower thighs, and upper thighs. The cuffs inflated sequentially during diastole cause retrograde aortic flow, and increased venous return. During end diastole, the cuffs rapidly deflate, resulting in unloading of the left ventricle and a decrease in systolic blood pressure. In addition there is also evidence that EECP improves endothelial function. Endothelial dysfunction with imbalance of vasodilatory and vasoactive substance is thought to contribute to elevated blood pressure. This leads us believe that EECP, although not used at present for patients with Resistant HTN, may represent a novel, valuable and untapped therapy.
We propose to study the effect of EECP therapy on mean ambulatory blood pressure and noninvasive hemodynamics in subjects with Resistant HTN. We will measure subjects' ambulatory blood pressure and noninvasive hemodynamics parameters at baseline, 4 weeks and 7 weeks. Subjects will undergo a 7 week course (35 sessions) of EECP therapy. Follow up ambulatory BP and non invasive hemodynamic parameters will be measured to evaluate any change in BP.
Our hypothesis is that in patients with Resistant HTN will demonstrate improved Blood pressure after completion of 35 sessions of EECP therapy.
- Conditions
- Hypertension
- Being tested
- Enhanced External Counterpulsation
- Keywords
- Resistant Hypertension, Endothelial dysfunction, Enhanced External Counterpulsation
- Medical subject headings
- Hypertension
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Enhanced External CounterpulsationDevice
A non-invasive method currently used for the treatment of ischemic coronary disease. During EECP therapy three compressive pneumatic cuffs are wrapped around the calves, lower thighs, and upper thighs. The cuffs inflate sequentially during diastole causing retrograde aortic flow, and increased venous return. At end diastole, the cuffs rapidly deflate resulting in unloading of the left ventricle and a decrease in systolic blood pressure.
What is being measured
The primary outcome is the main question the study is designed to answer.
Change from baseline in mean ambulatory 24-hour systolic ambulatory blood pressure
Measured: Approximately 50 days
Secondary outcomes (1)
Change from baseline in mean ambulatory 24-hour diastolic ambulatory blood pressure
Measured: Approximately 50 days
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 Aug 2009 (estimated)
- Study startMay 2009
- Primary completionOct 2011
- Study completionOct 2011
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for HypertensionStudies 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
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 0 participants (actual)
Sponsor and investigators
- Lead sponsor
- Albert Einstein Healthcare Network
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Darshak Karia, MD, Albert Einstein Healthcare Network
- Investigators
- Darshak H Karia, MD, Principal investigator, Albert Einstein Medical Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00953797
- Sponsor's protocol ID
- HN4112
- Acronym
- EECP
- Status last verified
- Jan 2012
- First submitted
- 5 Aug 2009
- Last updated
- 26 Jan 2012
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 26 Jan 2012. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Role of EECP Therapy in Patients With Resistant Hypertension
- ClinicalTrials.gov ID
- NCT00953797
- Acronym / sponsor ID
- EECP / HN4112
- Conditions
- Hypertension
- Keywords
- Resistant Hypertension, Endothelial dysfunction, Enhanced External Counterpulsation
- Study type
- Interventional
- Recruitment status
- Withdrawn
- Enrolment
- 0 participants (actual)
- Lead sponsor
- Albert Einstein Healthcare NetworkUniversity, hospital or other
- Study start
- May 2009
- Primary completion
- Oct 2011 (actual)
- Study completion
- Oct 2011 (actual)
- First posted
- 6 Aug 2009 (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.
High Blood Pressure or Hypertension is one of the main causes of stroke, heart disease, heart attack and kidney disease. Traditionally physicians use diet and lifestyles change and medications to control patient's blood pressure. There are however, some patients whose blood pressures are difficult to control and their blood pressure remains elevated despite multiple medications. When blood pressure remains above goal (greater then 140/90 or greater then 130/80 mmHg in patients with diabetes or kidney disease) despite 3 or more blood pressure medications, the investigators call it "Resistant Hypertension".
Enhanced External Counterpulsation (EECP) is a new method of treatment currently used in people with heart disease and chest pain. EECP therapy uses three sets of balloon like cuffs that are wrapped to the calves, lower thighs, and upper thighs. These cuffs inflate and deflate with every heart beat, causing increased blood return to the heart and better blood flow. It has also been found to improve the function of endothelial cells, a type of cells that lines the wall of blood vessel through out the body which helps to regulate and maintain blood pressure. This leads us to believe that EECP therapy, although not used at present for treating patients with Resistant Hypertension, may be useful in decreasing blood pressure.
Detailed description
Hypertension is a major cause and contributor to stroke, heart and kidney disease and could worsen the progression as well. Despite major reductions in age-adjusted death rates from coronary heart disease and stroke, these continue to be the leading and third most common causes of death, respectively, in the United States. In particular, for every 20 mm Hg increase in systolic blood pressure or 10 mm Hg in diastolic blood pressure, there is a doubling of stroke and coronary artery disease death rates. Kidney Failure related to hypertension continues to grow, especially among the African-American population.
Traditional approaches have mostly included pharmaceuticals targeting different mechanisms that contribute to HTN. However, adequate control of Blood pressure continues to remain a major problem.
Resistant hypertension is defined as blood pressure that remains above goal in spite of the concurrent use of three antihypertensive agents of different classes. Ideally, one of the three agents should be a diuretic and all agents should be prescribed at optimal dose amounts. Patients whose blood pressure is controlled but require four or more medications to do so should be considered resistant to treatment. The prevalence of resistant hypertension is unknown. Cross- sectional studies and hypertension outcome studies suggest, however, that it is not uncommon. In a recent analysis of National Health and Nutrition Examination Survey (NHANES) participants being treated for hypertension, only 53% were controlled to <140/90 mm Hg. In a cross-sectional analysis of Framingham Heart Study participants, only 48% of treated participants were controlled to <140/90 mm Hg and less than 40% of elderly participants (>75 years of age) were at a goal blood pressure.
The benefits of successful treatment, however, are likely substantial as suggested by hypertension outcome studies in general and by the early Veterans Administration cooperative studies, which demonstrated a 96% reduction in cardiovascular events over 18 months with use of triple antihypertensive regimens compared with placebo in patients with severe hypertension (diastolic blood pressure 115 to 129 mm Hg).
Furthermore, as age and obesity are the two most common risk factors for hypertension the prevalence will likely increase as the patient population gets older and heavier. This necessitates development of novel therapeutic approaches to blood pressure control.
Enhanced External Counterpulsation (EECP) is a non-invasive method currently used for the treatment of ischemic coronary disease. During EECP therapy three compressive pneumatic cuffs are wrapped to the calves, lower thighs, and upper thighs. The cuffs inflated sequentially during diastole cause retrograde aortic flow, and increased venous return. During end diastole, the cuffs rapidly deflate, resulting in unloading of the left ventricle and a decrease in systolic blood pressure. In addition there is also evidence that EECP improves endothelial function. Endothelial dysfunction with imbalance of vasodilatory and vasoactive substance is thought to contribute to elevated blood pressure. This leads us believe that EECP, although not used at present for patients with Resistant HTN, may represent a novel, valuable and untapped therapy.
We propose to study the effect of EECP therapy on mean ambulatory blood pressure and noninvasive hemodynamics in subjects with Resistant HTN. We will measure subjects' ambulatory blood pressure and noninvasive hemodynamics parameters at baseline, 4 weeks and 7 weeks. Subjects will undergo a 7 week course (35 sessions) of EECP therapy. Follow up ambulatory BP and non invasive hemodynamic parameters will be measured to evaluate any change in BP.
Our hypothesis is that in patients with Resistant HTN will demonstrate improved Blood pressure after completion of 35 sessions of EECP therapy.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
Who may qualify
- Ages
- 18 to 80 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (8 listed)
- Subjects who are competent to provide written consent
- Aged 18 to 80 years
- Deemed to be compliant with anti-hypertension medication therapy.
- Subjects with diabetes and/or chronic kidney disease must have a mean systolic blood pressure ≥130 mmHg
- All other subjects must have a mean systolic blood pressure ≥140 mmHg
Key exclusion criteria (25 listed)
- Average sitting systolic blood pressure ≥180 mmHg or diastolic blood pressure ≥110 mmHg
- Known Sleep apnea
- Subjects who have participated in a clinical study involving another investigational drug or device within 4 weeks prior to Screening
- Have hypertension secondary to an identifiable and treatable cause other than sleep apnea
- Acute coronary syndrome < 6 weeks prior to enrollment
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 CounterpulsationA non-invasive method currently used for the treatment of ischemic coronary disease. During EECP therapy three compressive pneumatic cuffs are wrapped around the calves, lower thighs, and upper thighs. The cuffs inflate sequentially during diastole causing retrograde aortic flow, and increased venous return. At end diastole, the cuffs rapidly deflate resulting in unloading of the left ventricle and a decrease in systolic blood pressure. | Device | – |
Primary outcome
Change from baseline in mean ambulatory 24-hour systolic ambulatory blood pressure
Time frame: Approximately 50 days
1 secondary outcome
Change from baseline in mean ambulatory 24-hour diastolic ambulatory blood pressure
Time frame: Approximately 50 days
Results and safety
The study was withdrawn before enrolling participants, so there are no results.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 26 Jan 2012.
Related trials for Hypertension
Active, not recruiting
Digital Reinforcement of Motivational Interviewing Micro-Skills Among Primary Care Healthcare Professionals
Hypertension (Without Type 2 Diabetes Mellitus)
Recruiting
Investigating Vascular Properties of HEMI and SPG Signals in Individuals With or at Risk for Chronic Kidney Disease
Chronic Kidney Disease, Hypertension (HTN)
Recruiting
Trial Phase: Syndemic Adapted Medly Uganda
Mental Health
Not yet recruitingPhase 2/3
An Open-Label Extension Study to Evaluate Inhaled Treprostinil SMI in Participants With Pulmonary Hypertension Associated With Chronic Obstructive Pulmonary Disease (PH-COPD)
Pulmonary Hypertension Associated With Chronic Obstructive Pulmonary Disease
Enrolling by invitation
Testing Implementation Strategies to Support Clinic Fidelity to an Outpatient Hypertension Bundle
Pregnancy Related, Hypertension
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.
Darshak H Karia, MD principal investigator
Albert Einstein Medical Center
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 Hypertension, run by Albert Einstein Healthcare Network at 1 site in United States.
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 25 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: withdrawn, as of the sponsor's last update on 26 Jan 2012. 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 United States. 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 was withdrawn before enrolling participants, so there are no results.
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?
Change from baseline in mean ambulatory 24-hour systolic ambulatory blood pressure (time frame: Approximately 50 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 26 Jan 2012.