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Clinical Trials/NCT00223626
NCT00223626
Completed
Phase 2

Lab Trials to Develop Medication for Cocaine Dependence

Bankole Johnson2 sites in 1 country25 target enrollmentJanuary 2007

Overview

Phase
Phase 2
Intervention
Topiramate
Conditions
Cocaine-Related Disorders
Sponsor
Bankole Johnson
Enrollment
25
Locations
2
Primary Endpoint
Cocaine-induced mood changes
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

Cocaine addiction is a serious health problem with no available medical treatment for preventing relapse. Topiramate, a medication which lowers dopamine levels, may have the ability to diminish cocaine cravings in addicts. The purpose of this study is to determine the effectiveness of topiramate in reducing cocaine's rewarding effects in individuals addicted to cocaine.

Detailed Description

GABA is an inhibitory neurotransmitter that is found primarily in the brain. High GABA levels result in low levels of dopamine, another neurotransmitter that is the brain's "feel good" chemical and which plays a primary role in cocaine drug addiction. Cravings for cocaine can be reduced by lowering dopamine levels. This makes topiramate, a GABA-altering medication, a potential treatment for cocaine addiction. This study will evaluate the subjective, behavioral, and physiological effects of topiramate in individuals addicted to cocaine. Potential participants will initially attend a 4- to 6-hour screening session. This will include review of medical and drug histories, standardized psychological questionnaires, a physical exam, and blood collection. Eligible participants will then be admitted to the inpatient clinic. During the first day of experiment, participants will receive instructions and information about the study procedures. They will also undergo a physical exam, an electrocardiogram, standardized psychological questionnaires, and blood and urine collection. A single test dose of cocaine will be administered intravenously to all participants to ensure safety with continuation in the study. Vital signs will be monitored hourly throughout the day. The experiment will last 25 days and will enroll 24 individuals addicted to cocaine. In this three-part experiment, participants will be admitted to the inpatient clinic for an 8-day study session. Following this session, they will be discharged from the clinic for a 1-week washout phase. Participants will then return to the inpatient clinic for another 8-day study session. The two study sessions will be identical. During both sessions, participants will first receive topiramate or placebo for 4 consecutive days. While continuing to receive topiramate or placebo, participants will then also receive intravenous cocaine or placebo for 3 consecutive days.Participants will be monitored by the study physician. Electrocardiograms will be used to monitor heart activity, and blood will be drawn frequently to monitor levels of cocaine and topiramate. Participants will complete standardized questionnaires several times each day to assess mood changes and cognitive function.

Registry
clinicaltrials.gov
Start Date
January 2007
End Date
December 2010
Last Updated
14 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Sponsor Investigator
Principal Investigator

Bankole Johnson

Chair of Psychiatry and Neurobehavioral Sciences

University of Virginia

Eligibility Criteria

Inclusion Criteria

  • Meets DSM-IV-TRTM diagnostic criteria for cocaine dependence
  • Subjects must be non-treatment seeking, cocaine-dependent or cocaine-abusing individuals who report taking cocaine at least once a month
  • In generally good health as confirmed by medical history, physical examination, electrocardiogram, laboratory screening tests, and vital signs
  • Must be able to take oral medication, adhere to the medication regimens, and be willing to return to the clinic for regular study visits
  • Must be able to read and understand all instructions, rating scales, and questionnaires in English
  • Must be willing to stay overnight at the University Clinical Psychopharmacology Laboratory (UCPL)
  • Must comply with the alcohol, tobacco, and drug-free environment regulations at the UCPL
  • If female, must be postmenopausal for at least 1 year, surgically sterile, or willing to use contraception throughout the study

Exclusion Criteria

  • History of mental illness, other than cocaine or nicotine dependence
  • History of mental retardation or neuropsychological functioning greater than 1.5 standard deviation below expected rang.
  • Clinically significant abnormalities found on the electrocardiogram
  • History of hypertension (blood pressure greater than 140/90 mm Hg) or systolic hypotension (blood pressure less than 90/75 mm Hg)
  • Resting pulse rate of greater than 90 beats per minute
  • Cerebrovascular accident or transient ischemic attack
  • Ischemic heart disease or heart attack
  • Symptomatic coronary artery disease or peripheral vascular disease
  • Cancer or history of cancer within the 5 years of study entry (other than basal cell carcinoma)
  • Kidney disease and/or impaired kidney function, as defined by an estimated creatinine clearance of 60 mL per minute

Arms & Interventions

Topiramate

Intervention: Topiramate

Placebo

Intervention: Topiramate

Outcomes

Primary Outcomes

Cocaine-induced mood changes

Time Frame: measured throughout cocaine and topiramate testing sessions

Effects of topiramate on cognitive function

Time Frame: measured throughout cocaine and topiramate testing sessions

Drug safety

Time Frame: measured throughout cocaine and topiramate testing sessions

Cardiovascular response to cocaine (measured throughout cocaine and topiramate testing sessions)

Time Frame: measured throughout cocaine and topiramate testing sessions

Secondary Outcomes

  • Physiological response (measured throughout cocaine and topiramate testing sessions)(measured throughout cocaine and topiramate testing sessions)

Study Sites (2)

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