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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00689572
Other study ID # 13419
Secondary ID 1R01DA021776-01A
Status Completed
Phase Phase 2
First received
Last updated
Start date July 2008
Est. completion date December 2013

Study information

Verified date August 2021
Source University of Virginia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will evaluate the efficacy of ondansetron compared with placebo in the treatment of cocaine dependence.


Description:

We propose to conduct a 9 week randomized, controlled clinical trial to evaluate the efficacy of ondansetron 4 mg twice daily compared with placebo (total N = 100/group × 2 groups = 200 individuals randomized, 400 total subjects will be consented), provided as an adjunct to manual-driven, structured CBT + BBCET in the treatment of cocaine dependence.


Recruitment information / eligibility

Status Completed
Enrollment 108
Est. completion date December 2013
Est. primary completion date December 2013
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Males and females who have given written informed consent. - Ages 18 years and above and, must weigh at least 40 Kg and no more than 140 Kg. - Good physical health as determined by a complete physical examination, an EKG within normal limits, and laboratory screening tests within acceptable parameters. - Current DSM-IV diagnosis of cocaine dependence. - At least one positive urine drug screen for cocaine at screen or baseline prior to randomization. - The pregnancy test for females at intake must be negative. - Literacy in English and ability to read, understand, and complete the ratings scales and questionnaires accurately, follow instructions, and make use of the behavioral treatments. - Answered an advertisement in the newspaper/radio/television, and expressing a wish to stop using cocaine. - Willing to participate in behavioral treatments for cocaine dependence. Exclusion Criteria: Please contact site for additional information

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Ondansetron
4 mg twice a day + Cognitive Behavioral Therapy + Brief Behavioral Enhancement Therapy
Placebo
twice a day + Cognitive Behavioral Therapy + Brief Behavioral Enhancement Therapy

Locations

Country Name City State
United States University of Virginia Center for Addiction Research and Education Charlottesville Virginia
United States University of Virginia Center for Addiction Research and Education Richmond Virginia

Sponsors (2)

Lead Sponsor Collaborator
University of Virginia National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cocaine Use by Self-report Participants were assessed up to three times weekly for up to 9 weeks to evaluate cocaine use by self-report up to 9 weeks
Primary Cocaine Use by Urine Benzoylecgonine Urine samples were collected up to three times weekly for up to 9 weeks to test for the major cocaine metabolite benzoylecgonine up to 9 weeks
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