Clinical Efficacy of Disulfiram in LAAM-Maintained Cocaine Abusers
Primary Purpose
Cocaine-Related Disorder, Opiate Dependence
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Placebo
Disulfiram
Disulfiram
Disulfiram
Sponsored by
About this trial
This is an interventional treatment trial for Cocaine-Related Disorder
Eligibility Criteria
Inclusion Criteria:
- Between the ages of 18-65 years.
- Are not currently enrolled in treatment.
- Participants must demonstrate opioid dependence, as evidenced by documentation of prior opioid agonist maintenance and/or have signs of withdrawal upon administration of naloxone (<0.8 mg, i.m.), and an opioid-positive urine screen.
- Participants also must be current users of cocaine with self-reported use of > 7 gm during the preceding 12 months, self-reported use of > 1 time/week in at least one month preceding study entry, and cocaine-positive urine screen.
- Participants must fulfill DSM-IV criteria for opioid and cocaine dependence.
Exclusion Criteria:
- current diagnosis of other drug or alcohol physical dependence (other than opiates, cocaine or tobacco)
- significant medical conditions such as abnormal liver function (with laboratory findings greater than three times normal).
- active hepatitis; hypertension; a current cardiac condition or high risk of cardiovascular disease; seizure disorders; or another significant underlying medical condition which would contraindicate disulfiram or LAAM treatment.
- meets DSM-IV psychiatric classifications for schizophrenia, bipolar disorder, or other psychotic disorders; exhibiting current suicidality or homicidality; current use of a prescribed psychotropic medication that cannot be discontinued.
- pregnancy.
Sites / Locations
- West Haven VA
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Placebo Comparator
Experimental
Experimental
Experimental
Arm Label
placebo disulfiram
disulfiram 62.5
disulfiram 125
disulfiram 250
Arm Description
placebo disulfiram (0 mg/day)
disulfiram at 62.5 mg/day
disulfiram at 125 mg/day
disulfiram at 250 mg/day
Outcomes
Primary Outcome Measures
Reductions in cocaine use as measured by urine toxicology and self-report
Secondary Outcome Measures
Predictors of treatment efficacy using DBH genotyping for disulfiram will be tested.
Full Information
NCT ID
NCT00580827
First Posted
December 25, 2007
Last Updated
March 30, 2020
Sponsor
Yale University
Collaborators
National Institute on Drug Abuse (NIDA)
1. Study Identification
Unique Protocol Identification Number
NCT00580827
Brief Title
Clinical Efficacy of Disulfiram in LAAM-Maintained Cocaine Abusers
Official Title
Clinical Efficacy of Disulfiram in LAAM-Maintained Cocaine Abusers
Study Type
Interventional
2. Study Status
Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
September 2003 (undefined)
Primary Completion Date
March 2004 (Actual)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Yale University
Collaborators
National Institute on Drug Abuse (NIDA)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This 18-week, randomized, double blind clinical trial provided treatment for 160 cocaine-dependent opioid addicts, aged 18-65 years. Participants were stabilized on LAAM maintenance during the first 4 weeks and cocaine use was assessed; participants were then stratified by level of cocaine use and randomly assigned to receive one of the following: placebo disulfiram (0 mg/day), disulfiram at 62.5 mg/day, disulfiram at 125 mg/day, or disulfiram at 250 mg/day. During induction onto LAAM, participants were administered increasing doses of LAAM plus placebo disulfiram on a thrice-weekly basis until maintenance doses of LAAM are attained. At the beginning of week 5, participants received LAAM plus disulfiram or placebo disulfiram according to their randomized assignments, and were maintained on these agents through week 16. At the end of the study, participants underwent detoxification from LAAM and active/placebo medication over a 4- to 6-week period. All participants received weekly 1-hour psychotherapy (Cognitive Behavioral Treatment) with experienced clinicians specifically trained to deliver the therapy and who received ongoing supervision. The primary outcomes were retention and reduction in opioid and cocaine use, as assessed by self-report and confirmed by thrice-weekly urinalyses. Secondary outcomes included reductions in other illicit drug and alcohol use, as well as improvements in psychosocial functioning.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cocaine-Related Disorder, Opiate Dependence
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
126 (Actual)
8. Arms, Groups, and Interventions
Arm Title
placebo disulfiram
Arm Type
Placebo Comparator
Arm Description
placebo disulfiram (0 mg/day)
Arm Title
disulfiram 62.5
Arm Type
Experimental
Arm Description
disulfiram at 62.5 mg/day
Arm Title
disulfiram 125
Arm Type
Experimental
Arm Description
disulfiram at 125 mg/day
Arm Title
disulfiram 250
Arm Type
Experimental
Arm Description
disulfiram at 250 mg/day
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Matched placebo.
Intervention Type
Drug
Intervention Name(s)
Disulfiram
Intervention Description
disulfiram at 62.5 mg/day for 12 weeks.
Intervention Type
Drug
Intervention Name(s)
Disulfiram
Intervention Description
Disulfiram at 125 mg/day for 12 weeks.
Intervention Type
Drug
Intervention Name(s)
Disulfiram
Intervention Description
disulfiram at 250 mg/day for 12 weeks.
Primary Outcome Measure Information:
Title
Reductions in cocaine use as measured by urine toxicology and self-report
Time Frame
14 weeks
Secondary Outcome Measure Information:
Title
Predictors of treatment efficacy using DBH genotyping for disulfiram will be tested.
Time Frame
14 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Between the ages of 18-65 years.
Are not currently enrolled in treatment.
Participants must demonstrate opioid dependence, as evidenced by documentation of prior opioid agonist maintenance and/or have signs of withdrawal upon administration of naloxone (<0.8 mg, i.m.), and an opioid-positive urine screen.
Participants also must be current users of cocaine with self-reported use of > 7 gm during the preceding 12 months, self-reported use of > 1 time/week in at least one month preceding study entry, and cocaine-positive urine screen.
Participants must fulfill DSM-IV criteria for opioid and cocaine dependence.
Exclusion Criteria:
current diagnosis of other drug or alcohol physical dependence (other than opiates, cocaine or tobacco)
significant medical conditions such as abnormal liver function (with laboratory findings greater than three times normal).
active hepatitis; hypertension; a current cardiac condition or high risk of cardiovascular disease; seizure disorders; or another significant underlying medical condition which would contraindicate disulfiram or LAAM treatment.
meets DSM-IV psychiatric classifications for schizophrenia, bipolar disorder, or other psychotic disorders; exhibiting current suicidality or homicidality; current use of a prescribed psychotropic medication that cannot be discontinued.
pregnancy.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
James Poling, Ph.D.
Organizational Affiliation
Yale University
Official's Role
Principal Investigator
Facility Information:
Facility Name
West Haven VA
City
West Haven
State/Province
Connecticut
ZIP/Postal Code
06516
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Clinical Efficacy of Disulfiram in LAAM-Maintained Cocaine Abusers
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