Effect of Clonidine on Responses to Imagery Scripts

Completed · Phase 1 · Has a placebo group

Conditions studied: Cocaine Abuse, Heroin Abuse

In brief

Background: \- Research has shown that clonidine, a drug originally prescribed to treat high blood pressure and some symptoms of opioid withdrawal, can help block stress-induced relapse to heroin and cocaine seeking in rats. However, it does not seem to block cue-induced relapse in rats. Researchers are interested in studying whether clonidine shows the same pattern of effects on stress- and cue-induced cravings for heroin or cocaine in humans. Objectives: \- To compare the ability of clonidine to reduce stress- and cue-induced cocaine and heroin craving in drug abusers. Eligibility: \- Individuals between 18 and 55 years of age who are current cocaine or heroin users. Design: * This study will consist of two visits: a screening visit to determine eligibility and an experimental/script session. * Before the script session, participants will provide urine and breath samples for testing. Participants will complete questionnaires to measure their current drug craving and days since last use of cocaine or heroin. * At the start of the script session, participants will receive a dose of clonidine or placebo as directed by the study researchers. Three hours after dosing, participants will be read four scripts (two neutral, one stress-inducing, and one drug-cue-related) with breaks in between each script. After each script, participants will respond to questions about levels of stress and craving. * Participants will provide saliva samples immediately before and during the script readings, and will also be measured for skin response to the scripts.

Key facts

Study ID
NCT00318760
Run by
National Institute on Drug Abuse (NIDA)
People needed
92
Starts
2005-06-14
Expected to finish
2013-08-07
Last updated by the study team
2018-04-05

Who can join

Age: 18 and older, up to 55. Sex: any. Healthy volunteers: not accepted.

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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