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Completed

NCT Number: NCT00842985

Dronabinol Interactions With Cognitive Enhancing Drug in Humans

Marijuana use is a major problem among veterans and non-veterans. A patient's use of marijuana while engaged in psychotherapy treatment may affect their memory and, therefore, limit their ability to benefit from treatment. This study is designed to test a new pharmacotherapy, modafinil, which has the potential to improve memory functioning in marijuana using individuals.

We hypothesize that modafinil treatment will decrease ratings of drug liking and improve cognitive measures, especially episodic memory.

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Key information

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

Department of Veterans Affairs Hospital

West Haven, Connecticut, 06516, United States

About this study

The impairment of episodic memory in marijuana abusers has important treatment implications. Since many treatments, including cognitive-behavioral therapy, strongly utilize episodic memory, marijuana use during treatment may lead to diminished treatment outcomes. In addition, lessened response inhibition may lead to elevated rates of drug relapse while in treatment. Consequently, a treatment which will improve episodic memory and response inhibition may lead to improved treatment outcomes in marijuana users. One such treatment is modafinil.This study will be a 4 session within-subjects, double-blind, crossover study evaluating the impact of modafinil (400 mg/day) on the cognitive, subjective, and physiological effects of marijuana. Across 4 sessions, subjects will be randomly assigned to receive either oral placebo, modafinil (400mg), dronabinol (15mg), or dronabinol and modafinil. Outcome measures will include physiological, cognitive, and subjective drug effects.

Currently this study complete and has been published.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • • Males and females between 18 and 55 years old will be eligible for this study.
  • Marijuana used at least once in last 2 months and at least 10 times in lifetime.
  • Subjects do not meet DSM-IV criteria for marijuana abuse or dependence.
  • Subjects are NOT seeking treatment for substance abuse or dependence.
  • Females must not be pregnant as determined by pregnancy screening, nor breast feeding, and must be using acceptable birth control methods other than oral contraceptive pills (OCP). Modafinil may cause OCP to be ineffective. Acceptable forms of birth control are condoms, diaphragms, and IUDs.
  • No alcohol or drugs 24 hours prior to testing session.
  • Subjects must agree to not drive to or from session.

Exclusion criteria

  • • History of heart disease, left ventricular hypertrophy, ischemic ECG changes, chest pain, arrhythmia, hypertension.
  • History of severe renal or hepatic diseases.
  • History of psychosis, schizophrenia or bipolar type I disorder.
  • History of seizure disorder.
  • Current diagnosis of alcohol and other drug dependence (other than nicotine).
  • A positive urine toxicology result for cocaine or opiates at intake.
  • Current use of over-the-counter or prescription psychoactive drugs (antidepressant, anxiolytics, antipsychotics, mood stabilizers, psychostimulants).
  • Liver function tests (ALT or AST) greater than 3 times normal.
  • Known allergy to modafinil or dronabinol.

Treatment and study plan

drug condition

Drug

Dronabinol (15mg) or Modafinil (400mg) or Dronabinol + Modafanil or placebo

Other names: Marinol, Provigil,

Primary outcomes

  1. CANTAB:CAmbridge Neuropsychological Test Automated Battery RVIP: Rapid Visual Information Processing

    Time frame: Once for each test session (4 total).

    CANTAB RVIP is one component of this computerized battery and is a measure of sustained attention with a working memory component.

    This study used two subscales of the RVIP.

    • RVP A' ( Target sensitivity, a measure of the ability to detect sequences.) The range is from 0-1; bad to good.
    • RVP B'' ( Response bias, which is a measure of the tendency to respond regardless of whether a target is present.

    The range is from -1 to +1 ; bad to good

    The numbers represent probabilities as units on a scale.

Sponsors and collaborators

Lead sponsor

Yale University

Other

Collaborators

  • National Institute on Drug Abuse (NIDA)
  • VA Office of Research and Development

Registry information

Official study title

Dronabinol Interactions in Humans

Important dates

Study start
2008
Primary completion
2009
Study completion
2009
First posted
Feb 12, 2009
Registry last updated
May 30, 2017

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.

Published trials that share one or more normalized conditions with this study.