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NCT00249405 · ClinicalTrials.gov registry record · Phase 2

Predicting Alcoholics' Treatment Responses to a Selective Serotonin Re-uptake Inhibitor (SSRI)

A Phase 2 study, sponsored by University of Cincinnati.

Completed
Registry status
Phase 2
Development phase
200
Enrollment target

NCT00249405: Completed Phase 2 study, sponsored by University of Cincinnati.

NCT00249405 is a Phase 2 study that has completed, run by University of Cincinnati. The registered enrollment target is 200 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (50% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00249405, a Phase 2 study, has completed, sponsored by University of Cincinnati.

COMPLETED
Registry status
Phase 2
Development phase
200 participants
Enrollment target

Study Summary

This study is being done to determine if citalopram is safe and effective in the treatment of alcohol dependence. A second purpose is to evaluate whether alcohol dependent individuals who differ in a specific genetic marker respond differently to citalopram. Citalopram is a drug approved by the U.S. Food and Drug Administration (FDA) for the treatment of depression. It belongs to a category of medications called selective serotonin re-uptake inhibitors or SSRIs. The U.S. FDA has not approved citalopram for the treatment of alcohol dependence. Therefore, it is being used "off-label" in this study.

Interventions

  • DRUG Citalopram + MI
  • BEHAVIORAL Placebo + MI

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2005-02
Est. Completion 2010-10
Phase Phase 2
University of Cincinnati

245 total trials

What the finished NCT00249405 record still lists

NCT00249405 is an interventional study that assigns participants to a tested intervention. The registered 200 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 (50% higher).

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

NCT00249405 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00249405 about?

NCT00249405 is a clinical study titled "Predicting Alcoholics' Treatment Responses to a Selective Serotonin Re-uptake Inhibitor (SSRI)". This study is being done to determine if citalopram is safe and effective in the treatment of alcohol dependence. A second purpose is to evaluate whether alcohol dependent individuals who differ in a specific genetic marker respond differently to citalopram. Citalopram is a drug approved by the U.S...

What is the current status of trial NCT00249405?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 200 participants. The study started on 2005-02. Estimated completion is 2010-10.

What interventions are being tested in trial NCT00249405?

The interventions under investigation include: Citalopram + MI (DRUG), Placebo + MI (BEHAVIORAL).

Who is sponsoring clinical trial NCT00249405?

This trial is sponsored by University of Cincinnati, which has 245 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00249405's enrollment target sits among peer trials

200 304th of 2000 higher than 1,652 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 NCT00249405, the US trial registry maintained by the National Library of Medicine. NCT00249405 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.