Physiological Effects of Grape Seed Extract in Diastolic Heart Failure (GRAPEVINE-HF)

June 2, 2017 updated by: Scott L. Hummel, University of Michigan

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

Study Type

Interventional

Enrollment (Actual)

15

Phase

  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Michigan
      • Ann Arbor, Michigan, United States, 48109
        • University of Michigan

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

46 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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
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:
  • resveratrol
  • grapes
  • wine
  • polyphenols
  • quercetin
  • anthocyanins
  • flavonoids
  • flavanols
  • flavonols
  • antioxidants
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:
  • resveratrol
  • grapes
  • wine
  • polyphenols
  • quercetin
  • anthocyanins
  • flavonoids
  • flavanols
  • flavonols
  • antioxidants

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
Ultrasound measure of conduit artery endothelial function
Pre-six weeks of investigational drug and placebo intervention
Brachial artery flow-mediated dilation (FMD)
Time Frame: Post-six weeks of investigational drug and placebo intervention
Ultrasound measure of conduit artery endothelial function
Post-six weeks of investigational drug and placebo intervention

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
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
Carotid-femoral pulse wave velocity
Time Frame: Pre-six weeks of investigational drug and placebo intervention
Pre-six weeks of investigational drug and placebo intervention
Maximal exercise capacity and oxygen consumption
Time Frame: Pre-six weeks of investigational drug and placebo intervention
Pre-six weeks of investigational drug and placebo intervention
Resting and post-exercise ventricular systolic and diastolic function
Time Frame: Pre-six weeks of investigational drug and placebo intervention
Standard and novel echocardiographic measures including strain/strain rate
Pre-six weeks of investigational drug and placebo intervention
Urinary 8-isoprostanes
Time Frame: Pre-six weeks of investigational drug and placebo intervention
Measure of oxidative stress
Pre-six weeks of investigational drug and placebo intervention
Heart failure related quality of life
Time Frame: Pre-six weeks of investigational drug and placebo intervention
Minnesota Living With Heart Failure Questionnaire
Pre-six weeks of investigational drug and placebo intervention
24-hour blood pressure
Time Frame: Post-six weeks of investigational drug and placebo intervention
Mean and diurnal variation
Post-six weeks of investigational drug and placebo intervention
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
Post-six weeks of investigational drug and placebo intervention
Heart failure related quality of life
Time Frame: Post-six weeks of investigational drug and placebo intervention
Minnesota Living With Heart Failure Questionnaire
Post-six weeks of investigational drug and placebo intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Scott L Hummel, MD, MS, University of Michigan

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 1, 2010

Primary Completion (Actual)

November 4, 2013

Study Completion (Actual)

February 24, 2014

Study Registration Dates

First Submitted

August 2, 2010

First Submitted That Met QC Criteria

August 18, 2010

First Posted (Estimate)

August 19, 2010

Study Record Updates

Last Update Posted (Actual)

June 6, 2017

Last Update Submitted That Met QC Criteria

June 2, 2017

Last Verified

June 1, 2017

More Information

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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