Prazosin for ETOH or Cocaine Craving
Stopped early · Not applicable · Has a placebo group
Conditions studied: Alcoholism, Cocaine Dependence
In brief
This double-blind placebo controlled crossover pilot trial will test the hypothesis that prazosin, an alpha-1 adrenergic receptor antagonist, reduces craving for their drug of choice in cocaine-dependent and alcohol-dependent veterans. Both the study medication period and the placebo period are each 4 weeks in duration.
Key facts
- Study ID
- NCT00240227
- Run by
- US Department of Veterans Affairs
- People needed
- 8
- Starts
- 2004-04-01
- Expected to finish
- 2009-01-01
- Last updated by the study team
- 2018-08-31
Who can join
Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age 18-70 years
- Current DSM-IV diagnosis of alcohol dependence or cocaine dependence with no use in last 30 days
- Capacity to provide informed consent
- Actively enrolled in chemical dependency treatment at VA Puget Sound English fluency
You may not qualify if…
- Evidence of significant abuse of opiates, PCP, sedatives or anxiolytics
- Suicidal ideation
- DSM IV diagnosis of bipolar mood disorder, schizophrenia or schizoaffective disorder
- Significant acute or chronic medical illness, including unstable angina, recent myocardial infarction, history of congestive heart failure, preexisting hypotension (systolic < 110), or orthostatic hypotension (systolic drop > 20mmHg after two minutes standing or any drop with dizziness), insulin-dependent diabetes mellitus; chronic renal or hepatic failure, pancreatitis, gout, M ni re's disease, benign positional vertigo, narcolepsy
- Concomitant use of alpha-1 antagonists History of prazosin-sensitivity Women who are pregnant, nursing infant(s), or of childbearing potential and not using a contraceptive method judged by the investigator to be effective
- Non-compliance with outpatient chemical dependency treatment
Where it is running
- VA Puget Sound Health Care System — Seattle, Washington, United States
Full record on ClinicalTrials.gov
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