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Polyphenol
Oligopin® for Metabolic Syndrome
N/A
Waitlist Available
Led By David Crowley, MD
Research Sponsored by Les Derives Resiniques et Terpeniques
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, day 42 and day 84
Awards & highlights
Summary
The safety and efficacy of Oligopin® will be compared against a placebo to evaluate the effect on metabolic risk factors in subjects with metabolic syndrome. During the 84-day study period it is hypothesized that HDL cholesterol will increase and systolic blood pressure will decrease therefore lowering CVD risk factors after supplementation with Oligopin®. Additionally, it is hypothesized that Oligopin® supplementation will reduce fasting glucose levels.
Eligible Conditions
- Metabolic Syndrome
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, day 42 and day 84
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, day 42 and day 84
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Fasting blood sugar level
Secondary study objectives
Alanine aminotransferase (ALT)
Aspartate transaminase (AST)
BMI
+32 moreTrial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Oligopin®Experimental Treatment1 Intervention
Oligopin® contains French Maritime Pine Bark Extract
Group II: PlaceboPlacebo Group1 Intervention
Placebo is a mixture of different inert compounds
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Oligopin®
2014
N/A
~60
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Who is running the clinical trial?
Les Derives Resiniques et TerpeniquesLead Sponsor
KGK Science Inc.Industry Sponsor
78 Previous Clinical Trials
6,120 Total Patients Enrolled
2 Trials studying Metabolic Syndrome
83 Patients Enrolled for Metabolic Syndrome
David Crowley, MDPrincipal InvestigatorKGK Science Inc.
35 Previous Clinical Trials
2,713 Total Patients Enrolled
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