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NCT00000811 · ClinicalTrials.gov registry record · Phase 2

A Study to Compare Different Drugs Used to Prevent Serious Bacterial Infections in HIV-Positive Children

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

Completed
Registry status
Phase 2
Development phase
690
Enrollment target

NCT00000811: Completed Phase 2 study, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

NCT00000811 is a Phase 2 study that has completed, run by National Institute of Allergy and Infectious Diseases (NIAID). The registered enrollment target is 690 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (419% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00000811, a Phase 2 study, has completed, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

COMPLETED
Registry status
Phase 2
Development phase
690 participants
Enrollment target

Study Summary

This study compares 2 different treatments administered to try to prevent serious bacterial infections (such as pneumonia) in HIV-positive children. A combination of drugs (azithromycin plus atovaquone) will be compared to sulfamethoxazole-trimethoprim (SMX/TMP) alone. This study also evaluates the long-term safety and tolerance of these different drugs. SMX/TMP is a commonly prescribed drug for the prevention of bacterial infections. However, the combination of azithromycin and atovaquone may be safer and more effective than SMX/TMP. This study compares the 2 treatments.

Interventions

  • DRUG Azithromycin
  • DRUG Atovaquone
  • DRUG Sulfamethoxazole-Trimethoprim

Trial Details

FieldValue
Enrollment Target 690 participants
Est. Completion 2001-11
Phase Phase 2

What the finished NCT00000811 record still lists

NCT00000811 is an interventional study that assigns participants to a tested intervention. The registered 690 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (419% higher).

The record links to 0 conditions, and to 3 interventions - of which Azithromycin is the first listed.

NCT00000811 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00000811 about?

NCT00000811 is a clinical study titled "A Study to Compare Different Drugs Used to Prevent Serious Bacterial Infections in HIV-Positive Children". This study compares 2 different treatments administered to try to prevent serious bacterial infections (such as pneumonia) in HIV-positive children. A combination of drugs (azithromycin plus atovaquone) will be compared to sulfamethoxazole-trimethoprim (SMX/TMP) alone. This study also evaluates the ...

What is the current status of trial NCT00000811?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 690 participants. Estimated completion is 2001-11.

What interventions are being tested in trial NCT00000811?

The interventions under investigation include: Azithromycin (DRUG), Atovaquone (DRUG), Sulfamethoxazole-Trimethoprim (DRUG).

Who is sponsoring clinical trial NCT00000811?

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 NCT00000811's enrollment target sits among peer trials

690 46th of 2000 higher than 1,954 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 NCT00000811, the US trial registry maintained by the National Library of Medicine. NCT00000811 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.