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Completed

NCT Number: NCT00958282

Treatment of Cocaine Dependence With Lisdexamfetamine

This protocol is a 2-group double-blind placebo-controlled outpatient study investigating lisdexamfetamine for treatment of cocaine dependence. The investigators plan to enroll 100 subjects in a 14-week trial. The primary objectives will determine changes in cocaine use and secondary objectives will be cocaine craving and impulsivity.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Ambulatory Research Center/Fairview University Psychiatry Dept

Minneapolis, Minnesota, 55454, United States

About this study

This 2-group, double-blind, placebo-controlled, 14-week study (N=100) will investigate the efficacy of cognitive behavioral therapy plus lisdexamfetamine vs. placebo to treat cocaine dependence. We hypothesize that lisdexamfetamine will reduce cocaine use (primary outcome), as well as cocaine craving and impulsivity (secondary outcomes) vs. placebo.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Eligible participants must:
  • Be treatment-seeking males or females between 18 and 65 years-of-age;
  • Understand the study procedures and provide written informed consent;
  • Be judged by the examining physician to be in generally good health with the exception of health problems related to acute drug use;
  • Meet DSM-IV criteria for cocaine-dependence.

Exclusion criteria

  • Exclusion criteria include:
  • DSM-IV diagnoses for current psychotic disorders, mood disorders (except substance-induced depression), anxiety disorders, ADHD, and other current substance dependence (except marijuana and nicotine dependence); subjects may not have physiological dependence upon alcohol requiring medical detoxification;
  • Current use of any prescription medications;
  • Females currently pregnant or nursing;
  • Current elevation of liver enzyme levels above twice normal limits;
  • Existing cardiovascular disease as determined by physician, EKG evaluation;
  • History of significant acute or chronic physical illness precluding participation;
  • History of hyperthyroidism, glaucoma, or seizures.

Treatment and study plan

lisdexamfetamine/Behavior Therapy

Drug

Placebo

Other

Primary outcomes

  1. Cocaine-positive Urine Results

    Time frame: 14 Weeks

    At each visit, subjects provided urine samples, which were analyzed for benzoylecgonine (BE; a cocaine metabolite). BE was assessed semi-quantitatively using the PROFILE® -V MEDTOXScan® Drugs of Abuse Test System, with cocaine positive tests equaling or exceeding 150 ng/mL.

Secondary outcomes

  1. Drug Craving

    Time frame: 14 Weeks

    On a weekly basis, patients completed measures of cocaine craving using the Minnesota Cocaine Craving Scale.

    The Minnesota Cocaine Craving Scale is a self report questionnaire and ranges from 0 to 100, 0 being "very little" to 100 being "very much".

Sponsors and collaborators

Lead sponsor

University of Minnesota

Other

Registry information

Official study title

Lisdexamfetamine Treatment for Cocaine Dependence

Important dates

Study start
2009
Primary completion
2013
Study completion
2013
First posted
Aug 13, 2009
Registry last updated
Sep 17, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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