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Role of Enhanced External Counterpulsation (EECP) Therapy in Patients With Resistant Hypertension

This study has been withdrawn prior to enrollment.
Sponsor:
Information provided by (Responsible Party):
Darshak Karia, MD, Albert Einstein Healthcare Network
ClinicalTrials.gov Identifier:
NCT00953797
First received: August 5, 2009
Last updated: January 25, 2012
Last verified: January 2012
  Purpose

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.


Condition Intervention
Hypertension
Device: Enhanced External Counterpulsation

Study Type: Interventional
Study Design: Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Role of EECP Therapy in Patients With Resistant Hypertension

Resource links provided by NLM:


Further study details as provided by Albert Einstein Healthcare Network:

Primary Outcome Measures:
  • Change from baseline in mean ambulatory 24-hour systolic ambulatory blood pressure [ Time Frame: Approximately 50 days ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Change from baseline in mean ambulatory 24-hour diastolic ambulatory blood pressure [ Time Frame: Approximately 50 days ] [ Designated as safety issue: No ]

Enrollment: 0
Study Start Date: May 2009
Study Completion Date: October 2011
Primary Completion Date: October 2011 (Final data collection date for primary outcome measure)
Intervention Details:
    Device: Enhanced External Counterpulsation
    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.
  Show Detailed Description

  Eligibility

Ages Eligible for Study:   18 Years to 80 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • 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

Exclusion Criteria:

  • 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%
  • 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)
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00953797

Locations
United States, Pennsylvania
Albert Einstein Medical Center
Philadelphia, Pennsylvania, United States, 19141
Sponsors and Collaborators
Albert Einstein Healthcare Network
Investigators
Principal Investigator: Darshak H Karia, MD Albert Einstein Medical Center
  More Information

No publications provided

Responsible Party: Darshak Karia, MD, Director of Heart Failure Services, Albert Einstein Healthcare Network
ClinicalTrials.gov Identifier: NCT00953797     History of Changes
Other Study ID Numbers: HN4112
Study First Received: August 5, 2009
Last Updated: January 25, 2012
Health Authority: United States: Institutional Review Board

Keywords provided by Albert Einstein Healthcare Network:
Resistant Hypertension
Endothelial dysfunction
Enhanced External Counterpulsation

Additional relevant MeSH terms:
Hypertension
Cardiovascular Diseases
Vascular Diseases

ClinicalTrials.gov processed this record on November 25, 2014