Double-Blind Naltrexone in Kleptomania
Completed · Phase 2 · Has a placebo group
Conditions studied: Kleptomania
In brief
The goal of the proposed study is to evaluate the efficacy and safety of naltrexone in kleptomania.
Key facts
- Study ID
- NCT00332579
- Run by
- University of Minnesota
- People needed
- 25
- Starts
- 2006-05-01
- Expected to finish
- 2008-09-01
- Last updated by the study team
- 2019-07-29
Who can join
Age: 21 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- men and women age 21-75
- current DSM-IV kleptomania.
You may not qualify if…
- unstable medical illness or clinically significant abnormalities on prestudy laboratory tests or physical examination
- history of seizures
- myocardial infarction within 6 months
- current pregnancy or lactation, or inadequate contraception in women of childbearing potential
- clinically significant suicidality
- current or recent (past 3 months) DSM-IV substance abuse or dependence
- illegal substance within 2 weeks of study initiation
- initiation of psychotherapy or behavior therapy from a mental health professional for the treatment of kleptomania within 3 months prior to study baseline
- initiation of a psychotropic medication within 2 months prior to study inclusion
- previous treatment with naltrexone
- treatment with investigational medication or depot neuroleptics within 3 months, with fluoxetine within 6 weeks, or with other psychotropics within 2 weeks prior to study baseline.
Where it is running
- University of Minnesota — Minneapolis, Minnesota, United States
Full record on ClinicalTrials.gov
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