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NCT01641159 · ClinicalTrials.gov registry record · Phase 2

Study of Buspirone for Relapse-Prevention in Adults With Cocaine Dependence

A Phase 2 study, sponsored by University of Cincinnati.

Completed
Registry status
Phase 2
Development phase
62
Enrollment target

NCT01641159 is a Phase 2 study that has completed, run by University of Cincinnati. The registered enrollment target is 62 participants.

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The verdict

NCT01641159, a Phase 2 study, has completed, sponsored by University of Cincinnati.

COMPLETED
Registry status
Phase 2
Development phase
62 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate whether or not buspirone is effective in preventing relapse in cocaine-dependent adults in inpatient/residential treatment who are planning to enter outpatient treatment upon inpatient/residential discharge.

Interventions

  • DRUG Placebo
  • DRUG Buspirone

Trial Details

FieldValue
Enrollment Target 62 participants
Start Date 2012-08
Est. Completion 2013-06
Phase Phase 2

Sponsor

University of Cincinnati

245 total trials

What the Registry Record Tells You About NCT01641159

The ClinicalTrials.gov registry entry for NCT01641159 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 62 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Cincinnati, which has 245 total studies on file at ClinicalTrials.gov.

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

NCT01641159 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01641159 about?

NCT01641159 is a clinical study titled "Study of Buspirone for Relapse-Prevention in Adults With Cocaine Dependence". The purpose of this study is to evaluate whether or not buspirone is effective in preventing relapse in cocaine-dependent adults in inpatient/residential treatment who are planning to enter outpatient treatment upon inpatient/residential discharge.

What is the current status of trial NCT01641159?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 62 participants. The study started on 2012-08. Estimated completion is 2013-06.

What interventions are being tested in trial NCT01641159?

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

Who is sponsoring clinical trial NCT01641159?

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

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.