Disulfiram for Treating Cocaine Dependence in Individuals Maintained on Methadone

Sponsor
University of Arkansas (Other)
Overall Status
Completed
CT.gov ID
NCT00218608
Collaborator
Yale University (Other)
158
1
4
69
2.3

Study Details

Study Description

Brief Summary

Cocaine is an extremely addictive stimulant drug that directly affects the brain. It is used in several different forms and can be snorted, smoked, or injected to achieve the desired effect. Cocaine users are at risk for many health problems, both directly and indirectly related to the effects of cocaine. Disulfiram, a drug used to treat chronic alcoholism, may be effective in reducing cocaine use. This study will evaluate the effectiveness of three different doses of disulfiram in treating cocaine dependence in opioid- and cocaine-dependent individuals maintained on methadone.

Condition or Disease Intervention/Treatment Phase
Phase 2

Detailed Description

Despite the harm that cocaine can cause to the body, its abuse is widespread. It is the cause of more visits to hospital emergency rooms nationwide than any other illegal drug. Effective treatments for cocaine and opiate addictions are essential to the decline of cocaine- and opiate-related disorders. Unfortunately, cocaine use remains prevalent among participants in many opioid maintenance programs. The addition of other medications to methadone maintenance may prove helpful in reducing cocaine use. Disulfiram, a drug used to treat chronic alcoholism, causes unpleasant effects when even small amounts of alcohol are consumed. This study will evaluate the effectiveness of three different doses of disulfiram in treating cocaine dependence in opioid- and cocaine-dependent individuals maintained on methadone.

Participants in this double blind study will be randomly assigned to receive either disulfiram at one of three dosage levels (62.5, 125, 250 mg/day) or placebo for 14 weeks. During the first 2 weeks, doses of methadone plus either disulfiram or placebo will be administered until the assigned maintenance dose is achieved. This dosage level will be maintained for the duration of the study. Participants will be required to report to the study site Monday through Saturday of each week for assessments and to receive medication. They will receive a take-home dose of medication for Sunday. In addition, participants will receive a weekly session of cognitive-behavioral therapy. Urine samples will be collected three times a week to assess drug use. At the end of the study, participants will undergo a 4- to 6-week detoxification period in which they will gradually discontinue the use of methadone and disulfiram. All participants have the option to request transfer to a local methadone maintenance program instead of undergoing detoxification.

Enrollment has been completed and no subjects are active. Data analyses are being conducted at this time.

Study Design

Study Type:
Interventional
Actual Enrollment :
158 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Disulfiram for Cocaine Abuse in Methadone- Patients
Study Start Date :
Apr 1, 2001
Actual Primary Completion Date :
Jan 1, 2007
Actual Study Completion Date :
Jan 1, 2007

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: Placebo

Placebo (microcrystalline cellulose) was suspended in the methadone during weeks 3-14.

Drug: Disulfiram
Disulfiram at 0, 62.5, 125 and 250 mg/day were administered during weeks 3-14
Other Names:
  • Antabuse
  • Active Comparator: Disulfiram at 62.5 mg

    Disulfiram at 62.5 mg was suspended in the methadone during weeks 3-14.

    Drug: Disulfiram
    Disulfiram at 0, 62.5, 125 and 250 mg/day were administered during weeks 3-14
    Other Names:
  • Antabuse
  • Active Comparator: Disulfiram at 125 mg

    Disulfiram at 125 mg/day was suspended in methadone during weeks 3-14.

    Drug: Disulfiram
    Disulfiram at 0, 62.5, 125 and 250 mg/day were administered during weeks 3-14
    Other Names:
  • Antabuse
  • Active Comparator: Disulfiram at 250 mg

    Disulfiram at 250 mg/day was suspended in methadone during weeks 3-14.

    Drug: Disulfiram
    Disulfiram at 0, 62.5, 125 and 250 mg/day were administered during weeks 3-14
    Other Names:
  • Antabuse
  • Outcome Measures

    Primary Outcome Measures

    1. Cocaine use [14 wks]

      Urine toxicology screens were conducted thrice-weekly for 14 weeks.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • History of cocaine use at least once a week during the month prior to study entry

    • Urine screen tests positive for cocaine

    • Meets DSM-IV criteria for opioid- and cocaine-dependence

    • Urine toxicology screen tests negative for benzodiazepines prior to beginning methadone treatment

    Exclusion Criteria:
    • Current drug or alcohol dependence other than opiates, cocaine, or tobacco

    • Significant medical condition, such as abnormal liver function (with laboratory findings greater than three times normal), active hepatitis, or high blood pressure

    • Current cardiac condition

    • Occult coronary artery disease

    • At high risk for cardiovascular disease, seizure disorders, or any other significant underlying medical condition that may make treatment with disulfiram or methadone unsafe

    • Meets DSM-IV psychiatric diagnostic criteria for lifetime schizophrenia, bipolar disorder, or other psychotic disorders

    • Currently suicidal or homicidal

    • Currently taking a prescribed psychotropic medication that cannot be discontinued

    • Pregnant

    • Currently taking metronidazole or clotrimazole

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Arkansas for Medical Sciences Little Rock Arkansas United States 72205 7911

    Sponsors and Collaborators

    • University of Arkansas
    • Yale University

    Investigators

    • Principal Investigator: Alison Oliveto, PhD, UAMS

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Arkansas
    ClinicalTrials.gov Identifier:
    NCT00218608
    Other Study ID Numbers:
    • NIDA-13441-1
    • R01-13441-1
    • DPMC
    First Posted:
    Sep 22, 2005
    Last Update Posted:
    Jan 31, 2012
    Last Verified:
    Jan 1, 2012
    Keywords provided by University of Arkansas
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 31, 2012