Ambulatory Research Center
Minneapolis, Minnesota, 55454, United States
NCT Number: NCT00927563
The goal of the proposed study is to evaluate the efficacy and safety of tolcapone in pathological gambling.
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Notify Me21 year–75 year
All sexes
Interventional
Phase 2
Minneapolis, Minnesota, 55454, United States
The proposed study will consist of 8 weeks of treatment with tolcapone in 10 subjects with pathological gambling. The hypothesis to be tested is that tolcapone will be effective in reducing the urges to gamble in patients with pathological gambling. The proposed study will provide needed data on the treatment of a disabling disorder that currently lacks a clearly effective treatment.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
pill, 100-300mg/day for 8 weeks
Other names: Brand name: TASMAR
Time frame: Visit 5 (final visit)
The overall impression of the clinician of the severity of the subject. Scores between 1 and 7 with 1 not being ill at all and 7 being one of the worst cases seen. CGI is assessed at every visit (1-5), but only the final visit will be reported here.
Time frame: Visit 5 (final visit)
Scale used to measure severity of gambling. Scores could range from 0-40 with 0 being the least severe and 40 being the most severe. Here the total score was used. The PG-YBOCS was completed at every visit (1-5), but the final visit (visit 5) will be the only score reported.
Time frame: Visit 5 (final visit)
Self report test of severity of gambling on a scale from 0-48 with 48 being the most severe. The G-SAS was performed at every visit (1-5), but only the final visit (visit 5) will be reported here as a final score.
University of Chicago
Other
Tolcapone Treatment of Pathological Gambling: An Open-Label Study
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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