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CompletedNCT00218166Updated Jan 11, 2017

Effectiveness of GABA Agonists in Reducing the Reinforcing Effects of Cocaine

A Phase 2 interventional study of GABA Agonists in Cocaine-Related Disorders, sponsored by National Institute on Drug Abuse (NIDA). Completed at 1 site in United States. Open to participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2017-01-11.

Sponsored by National Institute on Drug Abuse (NIDA) · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
78
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
All
01

Study summary

Cocaine abuse continues to represent a significant public-health concern. Cocaine likely creates its addictive effects by increasing levels of dopamine, a chemical found in the brain. GABA agonists are chemicals that have the opposite effect of cocaine by inhibiting the release of dopamine. The purpose of this study is to determine whether GABA agonists reduce the psychological and physiological reinforcing effects of cocaine.

Read the detailed description

Cocaine likely creates its reinforcing and addictive effects by increasing levels of dopamine, a brain neurotransmitter. GABA agonists are chemicals that have the opposite effect by inhibiting the release of dopamine. Increasing GABA activity may result in greater inhibition of dopamine systems, which may lead to new treatments for cocaine abuse. The purpose of this study is to determine whether pretreatment with GABA agonists reduces the psychological and physiological reinforcing effects of cocaine. Specifically, the study will look at three different GABA agonists: tiagabine, baclofen, and trazolam.

This double-blind, placebo-controlled study will involve three separate experimental phases; each phase will last 4 weeks and will test one of three GABA agonists (tiagabine, baclofen, or trazolam). Daily testing sessions will last approximately 6 hours. One of four GABA agonist dose treatments will be administered. Participants will then be introduced to a sample dose of intranasal cocaine. This will allow the participants to become acquainted with the drug effects of the corresponding cocaine dose for that day (0.444, 5, 10, or 20 mg). Subjective, physiological, and performance measures will be obtained. This will be followed by a period of cocaine self-administration. Participants will be given the opportunity to work on a computer to obtain additional single unit doses of cocaine. A total of 8 unit doses of cocaine will be available during each daily session. At the end of the daily session, additional subjective measures will be evaluated with questionnaires. Overall, a total of 16 GABA agonist-cocaine dose combinations will be administered on 16 different days. A subgroup of participants will also undergo similar procedures with the option to acquire money instead of cocaine. At the end of the study, all participants will be offered a referral to an appropriate drug-abuse treatment program.

02

Conditions studied

  • Cocaine-Related Disorders

Keywords

  • cocaine
  • tiagabine
  • baclofen
03

In context

Cocaine-Related Disorders

415 studies on the registry are indexed under Cocaine-Related Disorders; 12 are open to participants now.

This study's enrollment of 78 is above the median of 60 across 312 interventional studies indexed under Cocaine-Related Disorders.

Browse Cocaine-Related Disorders studies →

Lead sponsor

National Institute on Drug Abuse (NIDA) is the lead sponsor of 388 studies on the registry; 19 are open to participants now.

Of its 12 completed or terminated interventional studies of FDA-regulated products, 5 (42%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

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

Inclusion criteria

  • Recent use of cocaine
  • Meets DSM-IV diagnostic criteria for psychoactive substance abuse or dependence for cocaine
  • Positive drug urine screen for cocaine at time of initial screening interview
  • Reports self-administration of at least 1,260 mg of cocaine during the 4 weeks prior to study start date
  • Body Mass Index (BMI) of less than 29
  • Females must use an effective form of contraception throughout the study

Exclusion criteria

Exclusion Criteria:

  • Meets DSM-IV diagnostic criteria for psychoactive substance dependence for substances other than cocaine or nicotine
  • Currently seeking treatment for substance abuse/dependence
  • Current or past history of physical disease, impaired cardiovascular functioning, chronic obstructive pulmonary disease
  • History of seizure, head traumas, or central nervous system tumors
  • Current or past history of serious psychiatric disorder other than substance abuse or dependence
  • Family history of cardiovascular disease or seizure disorders
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Single group
Masking
Double (Participant, Care provider)
Enrollment
78 participants (actual)

Study arms

  • No intervention
    A

    Within subject design

    Drug: GABA Agonists

Interventions

  • DrugGABA Agonists

    GABA drugs administered acutely by mouth

    Also known as: Triazolam, tiagabine, baclofen

06

What researchers measure

Primary outcomes

  1. Progressive-ratio break point

    Time frame: Measured during each experimental session

Secondary outcomes

  1. Subjective effects of cocaine

    Time frame: Measured during each experimental session

  2. Physiological measures

    Time frame: Measured throughout the study

07

Study locations

1 site
  • University of Kentucky Medical Center
    Lexington, Kentucky 40536 0086, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 11, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00218166
Lead sponsor
National Institute on Drug Abuse (NIDA)
First posted
Sep 22, 2005
Start date
Aug 2001
Primary completion
May 2005
Completion
May 2005
Last update
Jan 11, 2017

Study contacts

Craig Rush
principal investigator · ACT

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2016. You cannot join it, but the record below documents what was studied.

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