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Completed

NCT Number: NCT00927563

Tolcapone Treatment of Pathological Gambling

The goal of the proposed study is to evaluate the efficacy and safety of tolcapone in pathological gambling.

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Key information

Age range

21 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Ambulatory Research Center

Minneapolis, Minnesota, 55454, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Men and women age 21-75;
  • Meet diagnostic criteria for current pathological gambling based on DSM-IV criteria and confirmed using the clinician-administered Structured Clinical Interview for Pathological Gambling (SCI-PG) (Grant et al., 2004);
  • Gambling behavior within 2 weeks prior to enrollment;
  • Women of child bearing age are required to have a negative result on a beta-human chorionic gonadotropin pregnancy test;
  • Women of childbearing potential utilizing a medically accepted form of contraception defined as double barrier, oral contraceptive, injectable contraceptive, implantable contraceptive devices, and abstinence.

Exclusion criteria

  • Infrequent gambling (i.e. less than one time per week) that does not meet DSM-IV criteria for PG;
  • Unstable medical illness or clinically significant abnormalities on laboratory tests, EKG, or physical examination at screen as determined by the investigator;
  • History of elevated liver enzymes (AST/ALT) or other liver abnormalities;
  • History of seizures;
  • Myocardial infarction within 6 months;
  • Current pregnancy or lactation, or inadequate contraception in women of childbearing potential;
  • A need for medication other than tolcapone with possible psychotropic effects or unfavorable interactions as determined by the investigator;
  • Clinically significant suicidality (defined as score 2 or higher on HAM-D item 3);
  • Current co-morbid Axis I disorder determined by the Structured Clinical Interview for DSM-IV (SCID), (First et al., 1995) - except for nicotine dependence;
  • Lifetime history of bipolar disorder type I or II, schizophrenia, or any psychotic disorder determined by SCID;
  • Clinically significant cognitive impairment (defined as score less than 88 on 3MS);
  • Current or recent (past 3 months) DSM-IV substance abuse or dependence;
  • Positive urine drug screen at screening;
  • Initiation of psychotherapy or behavior therapy for pathological gambling within 3 months prior to study baseline;
  • Previous treatment with tolcapone;
  • Treatment with an investigational medication or depot neuroleptics within 3 months;
  • Refusal to sign the tolcapone information sheet.

Treatment and study plan

Tolcapone

Drug

pill, 100-300mg/day for 8 weeks

Other names: Brand name: TASMAR

Primary outcomes

  1. Clinical Global Impression Scale (CGI)

    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.

Secondary outcomes

  1. Yale Brown Obsessive Compulsive Scale Modified for Pathological Gambling (PG-YBOCS)

    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.

  2. Gambling Symptom Assessment Scale (G-SAS)

    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.

Sponsors and collaborators

Lead sponsor

University of Chicago

Other

Registry information

Official study title

Tolcapone Treatment of Pathological Gambling: An Open-Label Study

Important dates

Study start
2009
Primary completion
2012
Study completion
2012
First posted
Jun 25, 2009
Registry last updated
Feb 23, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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