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Polyphenol
Dietary Supplement: resveratrol for Inflammation (MUresv Trial)
N/A
Waitlist Available
Led By James Smoliga, Ph.D.
Research Sponsored by Marywood University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 4 weeks, with optional additional 4 week treatment period
Awards & highlights
MUresv Trial Summary
The purpose of this study is to examine the effects of resveratrol on health and human performance. The study will evaluate cognitive function and several indicators of physical health before and after taking a resveratrol supplement or a placebo for three weeks.
MUresv Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 4 weeks, with optional additional 4 week treatment period
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4 weeks, with optional additional 4 week treatment period
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Vascular function
Secondary outcome measures
Body fat percentage
cognitive function
inflammation biomarkers
MUresv Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: Dietary Supplement: resveratrolActive Control1 Intervention
Subject will take resveratrol supplement for 4 weeks, with optional additional 4 week treatment period.
Group II: Sugar PillPlacebo Group1 Intervention
Subject will take placebo for daily for 4 weeks, with optional additional 4 week treatment period.
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Who is running the clinical trial?
Marywood UniversityLead Sponsor
6 Previous Clinical Trials
1,379 Total Patients Enrolled
2 Trials studying Inflammation
72 Patients Enrolled for Inflammation
James Smoliga, Ph.D.Principal InvestigatorMarywood University
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