- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01185067
Physiological Effects of Grape Seed Extract in Diastolic Heart Failure (GRAPEVINE-HF)
GRAPe Seed Extract and Ventriculovascular Investigation in Normal Ejection-Fraction Heart Failure
Diastolic heart failure (also known as "heart failure with normal ejection fraction" or "heart failure with preserved ejection fraction") occurs even though the heart muscle's pumping function is normal. In many cases diastolic heart failure is related to stiffening of the heart and blood vessels in people who have high blood pressure. Current guidelines suggest that patients should limit the salt content of their diet, as too much salty food can cause fluid retention and other problems in diastolic heart failure. Studies in animals with diastolic heart failure suggest that antioxidant chemicals found in grapes can block some of the harmful effects of salty diets. Because it is often difficult for patients with diastolic heart failure to maintain a low salt diet, the investigators are researching the effects of the antioxidant properties of grape seed extract, a natural supplement made from grape seeds. The investigators hypothesize that supplementing the diet with grape seed extract (GSE) can decrease the levels of harmful chemicals and improve heart and blood vessel function in patients with diastolic heart failure and a history of high blood pressure.
The University of Michigan research group plans to enroll 25 patients with a history of high blood pressure and diastolic heart failure in a research study. The study will assess the effects of GSE on hormones and other chemicals that can cause heart and blood vessel damage. The investigators will also study the effects of GSE on the ability of the blood vessels and heart muscles to relax at the proper time and speed. Finally, the investigators will observe how GSE affects participants' overall ability to exercise, quality of life, and blood pressure control. Study participants will be randomly assigned to take either GSE or placebo (looks like but does not contain GSE) capsules twice a day for six weeks. After a two-week break, all subjects will cross over to the opposite group of capsules for an additional six-week period. At the start of the study and at the end of each six-week time period study participants will have non-invasive heart and blood vessel testing, blood work and urine tests, and blood pressure monitoring.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Phase 1
Contacts and Locations
Study Locations
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Michigan
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Ann Arbor, Michigan, United States, 48109
- University of Michigan
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
Inclusion:
- Signs and symptoms of heart failure
- Left ventricular ejection fraction ≥ 50% (contrast ventriculography, echocardiography, nuclear scintigraphy, MRI or CT imaging)
- Diastolic dysfunction on previous echocardiogram/catheterization, or indeterminate diastolic function with supporting evidence of heart failure (HF) (as per European Society of Cardiology guidelines)
- History of systemic hypertension
- Age ≥ 50 years
- Willing to adhere to prescribed course of supplementation
- Informed consent
Exclusion Criteria:
- Daily intake of antioxidant supplements or vitamins beyond that provided in a standard daily multivitamin (e.g. high-dose vitamin E or vitamin C)
- NYHA Class IV heart failure symptoms (except during previous hospitalization)
- Hospitalization for decompensated heart failure within past one month
- Severely uncontrolled hypertension (SBP ≥ 180 and.or DBP ≥ 100 at rest, on current antihypertensive regimen
- Uncontrolled diabetes mellitus (hemoglobin A1C > 9%)
- Severe renal (estimated GFR < 30 ml/min) or hepatic disease/failure
- Severe anemia (Hgb < 9)
- Primary exercise limitation due to severe pulmonary disease
- Unacceptably poor echocardiographic images for analysis
- Worse than moderate mitral or aortic stenosis or insufficiency.
- Non-hypertensive cause of HFpEF (e.g. valvular disease, congenital heart disease, amyloidosis, sarcoidosis, constrictive pericardial syndromes)
- Myocardial infarction or unstable angina, including new or worsening anginal syndrome, within the past three months
- Uncontrolled arrhythmia (including non rate-controlled atrial fibrillation)
- Terminal illness expected to result in death within six months or active solid-organ cancer
- Psychiatric disorder (or dementia) with potential to compromise adherence
- Changes in medical regimen for heart disease or hypertension within past 1 month (except diuretic dose adjustment)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: grape seed extract capsule
Grape seed extract (MegaNatural BP, Polyphenolics, Inc.) 300 milligram capsules twice daily for six weeks
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Subjects will be randomized in double-blind fashion to either grape seed extract (GSE) or maltodextrin placebo capsules for for 6 weeks.
Patient will take 300 mg GSE/placebo twice a day for 6 weeks.
Patient will have a 2 week washout period and then cross over to the opposite group for an additional 6 weeks.
Other Names:
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Placebo Comparator: maltodextrin capsule
Maltodextrin capsules (matched for appearance and taste to grape seed extract capsules) twice daily for six weeks
|
Subjects will be randomized in double-blind fashion to either grape seed extract (GSE) or maltodextrin placebo capsules for for 6 weeks.
Patient will take 300 mg GSE/placebo twice a day for 6 weeks.
Patient will have a 2 week washout period and then cross over to the opposite group for an additional 6 weeks.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Brachial artery flow-mediated dilation (FMD)
Time Frame: Pre-six weeks of investigational drug and placebo intervention
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Ultrasound measure of conduit artery endothelial function
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Pre-six weeks of investigational drug and placebo intervention
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Brachial artery flow-mediated dilation (FMD)
Time Frame: Post-six weeks of investigational drug and placebo intervention
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Ultrasound measure of conduit artery endothelial function
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Post-six weeks of investigational drug and placebo intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
24-hour blood pressure
Time Frame: Pre-six weeks of investigational drug and placebo intervention
|
Mean and diurnal variation
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Pre-six weeks of investigational drug and placebo intervention
|
|
EndoPAT arterial endothelial function
Time Frame: Pre-six weeks of investigational drug and placebo intervention
|
Plethysmographic measure of resistance arterial endothelial function
|
Pre-six weeks of investigational drug and placebo intervention
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Carotid-femoral pulse wave velocity
Time Frame: Pre-six weeks of investigational drug and placebo intervention
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Pre-six weeks of investigational drug and placebo intervention
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|
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Maximal exercise capacity and oxygen consumption
Time Frame: Pre-six weeks of investigational drug and placebo intervention
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Pre-six weeks of investigational drug and placebo intervention
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|
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Resting and post-exercise ventricular systolic and diastolic function
Time Frame: Pre-six weeks of investigational drug and placebo intervention
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Standard and novel echocardiographic measures including strain/strain rate
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Pre-six weeks of investigational drug and placebo intervention
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Urinary 8-isoprostanes
Time Frame: Pre-six weeks of investigational drug and placebo intervention
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Measure of oxidative stress
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Pre-six weeks of investigational drug and placebo intervention
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Heart failure related quality of life
Time Frame: Pre-six weeks of investigational drug and placebo intervention
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Minnesota Living With Heart Failure Questionnaire
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Pre-six weeks of investigational drug and placebo intervention
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24-hour blood pressure
Time Frame: Post-six weeks of investigational drug and placebo intervention
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Mean and diurnal variation
|
Post-six weeks of investigational drug and placebo intervention
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|
EndoPAT arterial endothelial function
Time Frame: Post-six weeks of investigational drug and placebo intervention
|
Plethysmographic measure of resistance arterial endothelial function
|
Post-six weeks of investigational drug and placebo intervention
|
|
Carotid-femoral pulse wave velocity
Time Frame: Post-six weeks of investigational drug and placebo intervention
|
Post-six weeks of investigational drug and placebo intervention
|
|
|
Maximal exercise capacity and oxygen consumption
Time Frame: Post-six weeks of investigational drug and placebo intervention
|
Post-six weeks of investigational drug and placebo intervention
|
|
|
Resting and post-exercise ventricular systolic and diastolic function
Time Frame: Post-six weeks of investigational drug and placebo intervention
|
Standard and novel echocardiographic measures including strain/strain rate
|
Post-six weeks of investigational drug and placebo intervention
|
|
Urinary 8-isoprostanes
Time Frame: Post-six weeks of investigational drug and placebo intervention
|
Measure of oxidative stress
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Post-six weeks of investigational drug and placebo intervention
|
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Heart failure related quality of life
Time Frame: Post-six weeks of investigational drug and placebo intervention
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Minnesota Living With Heart Failure Questionnaire
|
Post-six weeks of investigational drug and placebo intervention
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Scott L Hummel, MD, MS, University of Michigan
Publications and helpful links
General Publications
- Sivaprakasapillai B, Edirisinghe I, Randolph J, Steinberg F, Kappagoda T. Effect of grape seed extract on blood pressure in subjects with the metabolic syndrome. Metabolism. 2009 Dec;58(12):1743-6. doi: 10.1016/j.metabol.2009.05.030. Epub 2009 Jul 15.
- Seymour EM, Singer AA, Bennink MR, Parikh RV, Kirakosyan A, Kaufman PB, Bolling SF. Chronic intake of a phytochemical-enriched diet reduces cardiac fibrosis and diastolic dysfunction caused by prolonged salt-sensitive hypertension. J Gerontol A Biol Sci Med Sci. 2008 Oct;63(10):1034-42. doi: 10.1093/gerona/63.10.1034.
- Ma L, Gao HQ, Li BY, Ma YB, You BA, Zhang FL. Grape seed proanthocyanidin extracts inhibit vascular cell adhesion molecule expression induced by advanced glycation end products through activation of peroxisome proliferators-activated receptor gamma. J Cardiovasc Pharmacol. 2007 May;49(5):293-8. doi: 10.1097/FJC.0b013e31803c5616.
- Kar P, Laight D, Rooprai HK, Shaw KM, Cummings M. Effects of grape seed extract in Type 2 diabetic subjects at high cardiovascular risk: a double blind randomized placebo controlled trial examining metabolic markers, vascular tone, inflammation, oxidative stress and insulin sensitivity. Diabet Med. 2009 May;26(5):526-31. doi: 10.1111/j.1464-5491.2009.02727.x.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Cardiovascular Diseases
- Vascular Diseases
- Heart Failure
- Heart Diseases
- Hypertension
- Heart Failure, Diastolic
- Physiological Effects of Drugs
- Molecular Mechanisms of Pharmacological Action
- Enzyme Inhibitors
- Platelet Aggregation Inhibitors
- Antineoplastic Agents
- Protective Agents
- Antineoplastic Agents, Phytogenic
- Antioxidants
- Quercetin
- Grape Seed Extract
- Resveratrol
Other Study ID Numbers
- HUM00029626
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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