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NCT00285584 · ClinicalTrials.gov registry record · Phase 1

Bupropion For Reducing High-Risk Behaviors in Depressed Men Who Have Sex With Men (MSM)

A Phase 1 study, sponsored by NYU Langone Health.

Completed
Registry status
Phase 1
Development phase
41
Enrollment target

NCT00285584: Completed Phase 1 study, sponsored by NYU Langone Health.

NCT00285584 is a Phase 1 study that has completed, run by NYU Langone Health. The registered enrollment target is 41 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (32% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00285584, a Phase 1 study, has completed, sponsored by NYU Langone Health.

COMPLETED
Registry status
Phase 1
Development phase
41 participants
Enrollment target

Study Summary

The primary purpose of this study was to test the whether high-risk, HIV-seronegative persons with mild-to-moderate depression would be more likely to adopt protective behavior change when provided with pharmacotherapy for their depression than when treated with placebo. High-risk behaviors include using illegal drugs and participating in unprotected sexual intercourse. The specific pharmacotherapy used in this study was the anti-depressant, bupropion. The subject population consisted of HIV negative men who have sex with men (MSM) with mild-to-moderate depression.

Primary Outcome

The self-reported number of partners in unprotected anal intercourse during the 3 months prior to interview as reported at the Month 6 visit minus reported at the enrollment visit.

Interventions

  • DRUG Placebo
  • DRUG Bupropion

Trial Details

FieldValue
Enrollment Target 41 participants
Start Date 2002-09
Est. Completion 2004-09
Phase Phase 1
NYU Langone Health

1,164 total trials

What the finished NCT00285584 record still lists

NCT00285584 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 41 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (32% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT00285584 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00285584 about?

NCT00285584 is a clinical study titled "Bupropion For Reducing High-Risk Behaviors in Depressed Men Who Have Sex With Men (MSM)". The primary purpose of this study was to test the whether high-risk, HIV-seronegative persons with mild-to-moderate depression would be more likely to adopt protective behavior change when provided with pharmacotherapy for their depression than when treated with placebo. High-risk behaviors include ...

What is the current status of trial NCT00285584?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 41 participants. The study started on 2002-09. Estimated completion is 2004-09.

What interventions are being tested in trial NCT00285584?

The interventions under investigation include: Placebo (DRUG), Bupropion (DRUG).

Who is sponsoring clinical trial NCT00285584?

This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00285584's enrollment target sits among peer trials

41 1125th of 2000 higher than 871 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT00285584, the US trial registry maintained by the National Library of Medicine. NCT00285584 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.