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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

Study Summary

A Study to Determine the Safety and Efficacy of Oligopin® on Metabolic Risk Factors in Subjects With Metabolic Syndrome

Eligible Conditions
  • Metabolic Syndrome

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, day 42 and day 84
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, day 42 and day 84 for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Fasting blood sugar level
Secondary outcome measures
Alanine aminotransferase (ALT)
Aspartate transaminase (AST)
BMI
+32 more

Trial 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

Find a Location

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

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~8 spots leftby Apr 2025