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CompletedNCT00276874Updated Apr 6, 2017

Aripiprazole to Reduce Cocaine Relapse

A Phase 1 interventional study of Aripiprazole and Placebos in Cocaine-Related Disorders, sponsored by Craig Rush. Completed at 1 site in United States. Open to participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2017-04-06.

Sponsored by Craig Rush · Phase 1, Interventional, and Treatment

Phase
Phase 1
Study type
Interventional
Enrollment
41
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
All
01

Study summary

Despite the many behavioral and cognitive treatment therapies that exist for cocaine addiction, individuals who complete cocaine abuse treatment are still at high risk for relapsing. Aripiprazole, a medication that is currently used to treat schizophrenia, may be useful in preventing drug relapse in individuals addicted to cocaine. This three-part study will evaluate the interaction between aripiprazole and cocaine. It will also determine the safety and effectiveness of aripiprazole in preventing drug relapse among cocaine addicts.

Read the detailed description

Cocaine addiction is a serious health problem with no available medical treatment for preventing relapse. Cocaine abusers often report that upon attempting to demonstrate control over the drug by only "sampling" it following a period of abstinence, they are more likely to relapse. These small "sampling" amounts of cocaine are thought to function as priming doses. Priming doses act as a stimulus in the brain to signal that there is more cocaine available, which in turn may lead to further cocaine use. Medications that reduce the stimulating effect of the cocaine priming dose may be useful in preventing cocaine relapse. Aripiprazole, a medication that is currently used to treat schizophrenia, may be effective at reducing relapse in individuals addicted to cocaine. By enhancing activity of the brain chemicals dopamine and serotonin, aripiprazole may counter the effects of cocaine and also reduce cocaine cravings.

This study will involve three sequential experiments. Experiment 1 will evaluate the physiological and behavioral effects of various combinations of cocaine and aripiprazole. Experiment 2 will evaluate the capability of aripiprazole at reducing the stimulating effects of cocaine. Lastly, Experiment 3 will evaluate the role of cocaine priming doses on subsequent cocaine use and how aripiprazole might alter the effect of the priming dose. In turn, these findings may lead to future clinical trials using aripiprazole to treat cocaine addiction and prevent relapse.

All three experiments will involve inpatient hospital stays. Participants will be required to refrain from using any non-study drugs, other than nicotine, and will undergo daily urine and breathalyzer tests. Questionnaires will be used to assess drug effects and cocaine cravings, and a computerized test will measure motor function and performance. Heart rate and blood pressure will be monitored periodically; an electrocardiogram (ECG) will record continuously to monitor heart electrical activity. Following the end of each experiment, all participants will be offered a referral to a drug abuse treatment program.

The first experiment will last 9 weeks and will enroll 8 individuals addicted to cocaine. Participants will take part in daily sessions in which they will receive varying doses of cocaine and aripiprazole, alone and in combination. This will provide important information regarding the safety and tolerability of cocaine-aripiprazole combinations.

The second experiment will last 10 weeks and will enroll 12 individuals addicted to cocaine. Participants will take part in various phases, which will each last several days. The phases will include a cocaine sampling phase; a cocaine acquisition phase in which participants will receive monetary rewards for distinguishing between cocaine and placebo; a placebo phase; an aripiprazole maintenance phase; a cocaine dose response phase in which the ability of aripiprazole to reduce cocaine's stimulating effects will be examined; and a washout phase in which no drugs will be given. Cocaine and aripiprazole doses will be determined by the results of the first experiment.

The third experiment will last 8 weeks and will enroll 12 individuals addicted to cocaine. A self-administration procedure designed to model relapse will be used to assess the effects of priming doses of cocaine on subsequent cocaine-taking behavior, alone and following aripiprazole treatment. Participants will be assigned to receive placebo for the first part of the study followed by aripiprazole for the remainder of the study or vice versa. During experimental sessions, participants will receive a specified amount of cocaine, which will act as the priming dose. Next, participants will choose between receiving either another similar dose of cocaine or money. This will be followed by a washout phase and then several more sampling-choice sessions with differing amounts of cocaine. Cocaine and aripiprazole doses will be determined by the results of the first experiment.

02

Conditions studied

  • Cocaine-Related Disorders

Keywords

  • Cocaine Addiction
  • Cocaine Dependence
03

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Meets DSM-IV diagnostic criteria for cocaine dependence
  • Current cocaine use at study entry, as determined by a urine screen
  • Body Mass Index of less than 30
  • ECG results within normal limits
  • If female, willing to use contraception throughout the study

Exclusion criteria

Exclusion Criteria:

  • Meets DSM-IV diagnostic criteria for dependence on any drugs other than cocaine or nicotine
  • Currently seeking treatment for substance abuse
  • Current or past serious illness, including impaired heart function, seizures, head trauma, or central nervous system tumors
  • A family history of heart disease or seizures
  • Current or past psychiatric disorder, other than substance abuse
  • Pregnant
04

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Triple (Participant, Care provider, Outcomes assessor)
Enrollment
41 participants (actual)

Study arms

  • Experimental
    Aripiprazole

    Subjects receive oral aripiprazole.

    Drug: Aripiprazole

  • Placebo comparator
    Placebo

    Subjects receive oral placebo

    Drug: Placebos

Interventions

  • DrugAripiprazole

    Aripiprazole; 0-30 mg; oral; daily

    Also known as: Abilify

  • DrugPlacebos

    Placebo; 0 mg; oral; daily

05

What researchers measure

Primary outcomes

  1. Behavioral effects of cocaine

    Time frame: Measured throughout the study

Secondary outcomes

  1. Heart rate; blood pressure; ECG

    Time frame: Measured throughout the study

06

Study locations

1 site
  • University of Kentucky
    Lexington, Kentucky 40506, United States
07

Registry details

Key details

Study ID
NCT00276874
Lead sponsor
Craig Rush
Collaborators
National Institute on Drug Abuse (NIDA)
Responsible party
Craig Rush (Principal Investigator, University of Kentucky) — Sponsor-investigator
First posted
Jan 13, 2006
Start date
Jan 2006
Primary completion
Jan 2012
Completion
Jan 2012
Last update
Apr 6, 2017

Study contacts

Craig R. Rush, PhD
principal investigator · University of Kentucky
Paul E Glaser, MD, PhD
principal investigator · University of Kentucky
Lon R. Hays, MD
principal investigator · University of Kentucky
Joshua A. Lile, PhD
principal investigator · University of Kentucky

Oversight

Data monitoring committee
Yes
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