Effects of Resveratrol Supplements on Vascular Health in Postmenopausal Women
NCT ID: NCT01564381
Last Updated: 2017-07-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE1/PHASE2
64 participants
INTERVENTIONAL
2012-03-31
2015-03-31
Brief Summary
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Detailed Description
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The "French Paradox" refers to diet patterns that, despite being high in saturated fat, are associated with a relatively low cardiovascular risk. An important aspect of many of the diets that were identified in the French Paradox studies is a significant intake of wine, particularly red wine, which can contain an array of phytochemicals that have been postulated to improve cardiovascular health. A polyphenolic that has received particular attention is this regard is resveratrol.
The stilbene resveratrol is found predominately in red grapes, red wine, peanuts and some berries, and it has been touted in the popular press for its potential health-promoting benefits. Emerging evidence suggests a role for resveratrol in the protection against numerous degenerative health problems including CVD and certain cancers, diabetes and some forms of neurodegeneration.
The amount of resveratrol in most foods is very low; thus obtaining the amounts of this compound that have been associated with improved health in animal models is difficult for humans. ResA is a product produced using patented technology that physically binds resveratrol to arginine, creating a novel conjugate. In the preliminary studies the ResA conjugate produced higher peak plasma levels, as well as total plasma levels that persist for a longer period of time when fed to rats. Whether similar results would occur in humans, and the extent to which increasing blood resveratrol concentration can be associated with positive cardiovascular effects in an at-risk population is the subject of this project.
Conditions
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Study Design
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RANDOMIZED
CROSSOVER
PREVENTION
DOUBLE
Study Groups
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Resveratrol
The capsules will contain 90mg of resveratrol.
Resveratrol
90mg of resveratrol.
ResA
ResA is a product produced by using patented technology that physically binds resveratrol to arginine, creating a novel conjugate. The capsules will contain 90mg of resveratrol.
ResA
90mg of resveratrol conjugated with arginine.
Placebo
The placebo will be cellulose.
Placebo
Made up of cellulose.
Interventions
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ResA
90mg of resveratrol conjugated with arginine.
Resveratrol
90mg of resveratrol.
Placebo
Made up of cellulose.
Eligibility Criteria
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Inclusion Criteria
* Lack of menses in the last year and FSH 23-116.3 mlU/mL
* Subject is willing and able to comply with the study protocols.
* Subject is willing to consume resveratrol supplements/placebo capsules on three separate occasions.
* BMI 18.5-34.9 kg/m2
* Weight ≥ 110 pounds
* LDL-C ≥ 130 mg/dL
Exclusion Criteria
* Self reported use of anticoagulation agents including NSAIDs
* Self reported use of oral cortisone or other immunosuppressive agents,
* Self reported underlying neoplasia or immunological disease
* Food faddists or those taking a non-traditional diet
* Self reported physical activity restricted or reduced due to chronic health conditions
* Self reported diabetes
* Blood pressure ≥ 140/90 mm Hg
* PFA-100 readings 10 % outside of normal reference range (normal reference range for ADP-Collagen: 71-118 sec; Epinephrine-Collagen: 94-193 sec).
* Self reported renal or liver disease
* Self reported heart disease, which includes cardiovascular events and stroke
* Self reported Cushing's syndrome
* Self reported chronic/routine high intensity exercise
* Inability to properly place or wear the PAT probes or abnormal measurements on pre-screening PAT
* Abnormal Liver, CBC or Chemistry panels (laboratory values outside the reference range) if determined to be clinically significant.
* Self reported cancer within past 5 years
* Self reported history of psychiatric disorders i.e. schizophrenia or bi-polar or depression treated with antidepressants within the last 1 year.
* Self reported use of MAOI inhibitor within the last 1 year (e.g. phenelzine (Nardil), tranylcypromine (Parnate), etc)
* Self reported malabsorption (e.g. difficulty digesting or absorbing nutrients from food,
50 Years
70 Years
FEMALE
Yes
Sponsors
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Gateway Health Alliance
INDUSTRY
University of California, Davis
OTHER
Responsible Party
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Principal Investigators
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Robert M Hackman, PhD
Role: PRINCIPAL_INVESTIGATOR
University of California, Davis
Locations
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University of California, Davis - Ragle Human Nutrition Research Center
Davis, California, United States
Countries
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Other Identifiers
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270881
Identifier Type: -
Identifier Source: org_study_id
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