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NCT00000925 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

Completed
Registry status
Phase 2
Development phase
56
Enrollment target

NCT00000925: Completed Phase 2 study, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

NCT00000925 is a Phase 2 study that has completed, run by National Institute of Allergy and Infectious Diseases (NIAID). The registered enrollment target is 56 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (58% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00000925, a Phase 2 study, has completed, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

COMPLETED
Registry status
Phase 2
Development phase
56 participants
Enrollment target

Study 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.

Interventions

  • DRUG Optimune oral nutritional supplement

Trial Details

FieldValue
Enrollment Target 56 participants
Start Date 1999-05
Phase Phase 2

What the finished NCT00000925 record still lists

NCT00000925 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 56 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (58% lower).

The record links to 0 conditions, and to 1 intervention - of which Optimune oral nutritional supplement is the first listed.

NCT00000925 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00000925 about?

NCT00000925 is a clinical study titled "A Study to Evaluate High Protein Supplementation in HIV-Positive Patients With Stable Weight Loss". 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 o...

What is the current status of trial NCT00000925?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 56 participants. The study started on 1999-05.

What interventions are being tested in trial NCT00000925?

The interventions under investigation include: Optimune oral nutritional supplement (DRUG).

Who is sponsoring clinical trial NCT00000925?

This trial is sponsored by National Institute of Allergy and Infectious Diseases (NIAID), which has 2,006 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00000925's enrollment target sits among peer trials

56 1146th of 2000 higher than 848 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00000925, the US trial registry maintained by the National Library of Medicine. NCT00000925 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.