Clinical Trials Directory

Trials / Completed

CompletedNCT00000925

A Study to Evaluate High Protein Supplementation in HIV-Positive Patients With Stable Weight Loss

Evaluation of High Protein Supplementation in HIV-1-Positive Subjects With Stable Weight Loss

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
56 (planned)
Sponsor
National Institute of Allergy and Infectious Diseases (NIAID) · NIH
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether a high-quality protein food supplement will help HIV-positive patients maintain, and possibly gain, muscle mass. Many HIV-positive patients lose weight that they are then unable to regain. This may be because patients are not eating enough protein or are not eating the right kinds of protein. The protein eaten in foods (such as meat, eggs, or beans) may not be able to make up for the amount of protein lost due to HIV infection. This study gives patients high-quality protein food supplements to help them maintain and/or gain weight.

Detailed description

In many HIV-infected individuals with prior weight loss, the failure to regain weight and lean tissue is at least in part the consequence of inadequate protein intake or ingestion of a poor-quality protein rather than total caloric intake. Dietary sources of protein are presumably inadequate to meet the high metabolic needs caused by HIV infection. To achieve a target protein intake in the range (1.5 to 2.0 g/kg/day) demonstrated in other catabolic diseases necessary to achieve positive nitrogen balance and to generate substantial anabolic effects, this study will administer a supplement containing high-quality protein. Two groups of 28 patients each are randomly chosen to receive either an oral nutritional supplement (Optimune) containing increased amounts of high-quality protein (whey), which is rich in cysteine and glutamine, or an isocaloric, identical-tasting supplement without added whey protein or amino acid supplementation. Weight, body composition, anthropometry, dietary intake, and general physical health are assessed at baseline and at Weeks 6 and 12. Plasma cysteine, glutathione, C-reactive protein, and prealbumin, along with urine IL-6, sTNFrII, and IL-1ra, are assessed at baseline and at Week 12.

Conditions

Interventions

TypeNameDescription
DRUGOptimune oral nutritional supplement

Timeline

Start date
1999-05-01
Primary completion
2003-06-01
First posted
2001-08-31
Last updated
2013-07-29

Locations

19 sites across 2 countries: United States, Puerto Rico

Source: ClinicalTrials.gov record NCT00000925. Inclusion in this directory is not an endorsement.