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Early Phase II Trials for Cocaine Medication Development - 1

Early Phase II Trials for Cocaine Medication Development

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00000317
Enrollment
31
Registered
1999-09-21
Start date
1996-08-31
Completion date
1999-07-31
Last updated
2017-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cocaine-Related Disorders, Substance-Related Disorders

Keywords

Cocaine, METHADONE PATIENTS, RISPERIDONE

Brief summary

The purpose of this study is to develop models for early Phase II testing of potential medications for cocaine dependence: amoxapine, risperidone and other agents. The study was a controlled pilot trial of risperidone in opiate-dependent patients on methadone maintenance. The study explored whether risperidone reduced cocaine use, cocaine craving, and cocaine subjective effects in patients on methadone maintenance who abused cocaine and whether it had an acceptable side effect profile. This

Detailed description

This was an 18-week prospective, randomized, placebo-controlled crossover design with placebo lead-in phase and terminal placebo phase. After two weeks of single-blind placebo, patients were randomly assigned to one of two schedules of medication: 2 Week Baseline Weeks 1-6 Weeks 7-12 Weeks 13-18 Group 1 placebo risperidone placebo placebo Group 2 placebo placebo risperidone placebo The first 6-week phase provided an initial double-blind medication-placebo comparison. In the second six-week phase (weeks 7-12), patients crossed over to the opposite treatment. During weeks 13-18, Group 1 patients remained on placebo while Group 2 patients were tapered from risperidone to placebo. For six weeks after the end of the trial, patients were offered routine clinical treatment with counseling and psychiatrist visits as needed. Medication dosage was titrated upwards on a fixed-flexible schedule to a maximum dose of 4 mg per day. Medication began at ½ mg risperidone for 3 days, then 1 mg for four days, 2 mg per day during week 2, 3 mg per day during week 3, and 4 mg per day during weeks 4-6. The titration schedule for risperidone in weeks 7-12 was the same as for weeks 1-6. In addition to treatment as usual, patients received a modified manual-guided relapse prevention counseling program in weekly meetings lasting approximately 20 minutes; these sessions provided cognitive and behavioral skills that were found to be helpful to patients in reducing cocaine use.

Interventions

DRUGRisperidone

Risperidone (4mg/day)

DRUGPlacebo

Placebo

BEHAVIORALRelapse prevention counseling

Modified manual guided relapse prevention counseling. Weekly 20 minute sessions consisting of cognitive behavioral skills. Both arms will receive this intervention.

Sponsors

National Institute on Drug Abuse (NIDA)
CollaboratorNIH
Research Foundation for Mental Hygiene, Inc.
CollaboratorOTHER
New York State Psychiatric Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

Inclusion: 1. good standing at methadone maintenance program 2. DSM-IV criteria for cocaine dependence or abuse 3. used cocaine at least 4 times in last month 4. able to give informed consent

Exclusion criteria

1. currently meets DSM-IV criteria for Major depression or dysthymia 2. meets DSM-IV criteria for attention deficit hyperactivity disorder, bipolar disorder, schizophrenia or any psychotic disorder 3. history of seizures 4. history of allergic reaction to risperidone 5. chronic organic mental disorder 6. significant current suicidal risk 7. pregnancy, lactation or failure to use adequate birth control (for females) 8. unstable physical disorders that may make participation hazardous 9. coronary vascular disease 10. cardiac conduction system disease as indicated by QRS duration \>/= 0.11 11. current use of other prescribed psychotropic medications 12. history of failure to respond to a previous adequate trial of risperidone 13. history of neuroleptic malignant syndrome, tardive dyskinesia, or severe extrapyramidal reactions to neuroleptic medications 14. current DSM-IV criteria for another substance dependence other than nicotine.

Design outcomes

Primary

MeasureTime frameDescription
Side effects1x/week for 18 weeksUsing the Modified Systemic Assessment for Treatment Emergent Effects the psychiatrist assessed side effects
Craving3x/week during 18 weeks of trialsubjective cravings were recorded on the Cocaine craving scale
Drug use3x/week during 18 weeks of trialurine drug testing and self reported use on the Substance Use Weekly Inventory
Retention18 weeks or length of study participationduration of individuals in the study.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026