Clinical Trials Directory

Trials / Completed

CompletedNCT00152893

To Determine if Chromium Nicotinate Supplementation Will Improve Insulin Resistance in HIV Patients With Metabolic Abnormalities

The Effects of Chromium Supplementation on Glucose and Lipid Metabolism in Patients With HIV Infection

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
52 (actual)
Sponsor
Johane Allard · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

In HIV patients, fasting insulin levels decrease with chromium supplementation. This study is to determine if chromium nicotinate supplementation at 400ug/day for 16 weeks will improve insulin resistance in HIV patients with metabolic abnormalities.

Detailed description

This study is a randomized, double-blind, placebo-controlled, crossover study where patients will be supplemented for 16 weeks with either chromium nicotinate 400 ug/day or placebo and then crossover to the opposite treatment for another 16 weeks. Each soft gel capsule of chromium contains 200ug of chromium and patients will take 1 capsule twice a day or its placebo. Placebo contains di-calcium phosphate in a soft gel capsule and its appearance is similar to the chromium capsules.

Conditions

Interventions

TypeNameDescription
DRUGchromium nicotinate
DRUGPlacebo

Timeline

Start date
2002-08-01
Primary completion
2008-02-01
Completion
2008-02-01
First posted
2005-09-09
Last updated
2013-07-19

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT00152893. Inclusion in this directory is not an endorsement.