CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 45 enrolled
Drug / intervention
Buspirone +1 moredrug
Likely dose
Buspirone 10 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02132832
NCT02132832Phase 2Completed

Buspirone, Stress, and Attentional Bias to Marijuana Cues

The University of Texas Health Science Center, Houston·interventional·Posted May 7, 2014·Updated Jun 2, 2017

In Brief

A Phase 2 clinical trial evaluating Buspirone and Placebo for Cannabis Use Disorder. Completed, enrolled 45 participants across 1 site.

Detailed Summary

This project has two primary goals. The first goal is to further scientific understanding about marijuana abuse by examining two recognized factors in marijuana use and relapse: (1) stress/anxiety and (2) atypical reactivity to marijuana-related stimuli (e.g., attentional bias). The second goal is to attenuate the influence of stress/anxiety and attentional bias to marijuana stimuli via administration of buspirone. Buspirone is uniquely suited to this project because it has effects on neurotransmitter systems known to modulate both stress/anxiety and attentional bias.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 2CompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedMay 7, 2014
Enrollment StartJun 1, 2013
Primary CompletionMar 1, 2016
TodayJul 2, 2026
Enrollment to primary: 2.8 yearsPosted 12.2 years ago

Interventions

Buspironedrug

Buspirone is an anxiolytic compound marked by modulation of both 5-HT1A and D3 receptors. Buspirone is administered orally twice per day (9:00 AM and 6:00 PM) for 3 weeks. 10 mg buspirone is administered on days 1-4, then the dose is increased by 10 mg every 3 days to a maximum of 40 mg buspirone on days 10-19.

Placebodrug

Placebo is administered orally twice per day (9:00 AM and 6:00 PM) for 3 weeks.