Clinical Trials Directory

Trials / Completed

CompletedNCT02129595

Resveratrol and First-degree Relatives of Type 2 Diabetic Patients

Effects of Resveratrol on Insulin Sensitivity, Brown Adipose Tissue and Metabolic Profile in First-degree Relatives of Type 2 Diabetic Patients

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
15 (actual)
Sponsor
Maastricht University Medical Center · Academic / Other
Sex
Male
Age
40 Years – 70 Years
Healthy volunteers
Not accepted

Summary

The main objective of the study is to investigate if resveratrol supplementation can improve overall and muscle-specific insulin sensitivity in first-degree relatives of type 2 diabetic patients. As a secondary objective the investigators want to investigate whether the improved insulin sensitivity can be attributed to improved muscle mitochondrial oxidative capacity and a reduced intrahepatic and cardiac lipid content. Furthermore, in a subset of the participants the investigators want to investigate the effect of resveratrol on glucose uptake in brown adipose tissue.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTplaceboA placebo will given for 30 days or 34 days (if included in brown adipose tissue measurement), twice daily. One pill will be provided with lunch, and the other pill will be provided with dinner.
DIETARY_SUPPLEMENTresveratrolresveratrol will be given for 30 days or 34 days (if included in brown adipose tissue measurement), twice daily. One pill, which contains 75 mg of resveratrol, will be provided with lunch, and the other pill, also containing 75 mg will be given with dinner. So in total a dose of 150 mg/day will be given.

Timeline

Start date
2014-04-01
Primary completion
2017-04-01
Completion
2017-07-31
First posted
2014-05-02
Last updated
2017-08-08

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT02129595. Inclusion in this directory is not an endorsement.