Dronabinol Interactions With Cognitive Enhancing Drug in Humans

NCT ID: NCT00842985

Last Updated: 2017-05-30

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

EARLY_PHASE1

Total Enrollment

53 participants

Study Classification

INTERVENTIONAL

Study Start Date

2008-09-30

Study Completion Date

2009-10-31

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Cannabis Marijuana Abuse

Study Design

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Intervention Model

SEQUENTIAL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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drug condition

Participants received each drug condition in sequential order across 4 test days. Not all participants received the interventions in the same order.

Group Type OTHER

drug condition

Intervention Type DRUG

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

Interventions

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drug condition

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

Intervention Type DRUG

Other Intervention Names

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Marinol, Provigil,

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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VA Office of Research and Development

FED

Sponsor Role collaborator

National Institute on Drug Abuse (NIDA)

NIH

Sponsor Role collaborator

Yale University

OTHER

Sponsor Role lead

Responsible Party

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Mehmet Sofuoglu

M.D., Ph.D.

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Mehmet Sofuoglu, M.D,Ph.D.

Role: PRINCIPAL_INVESTIGATOR

Yale University

Locations

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Department of Veterans Affairs Hospital

West Haven, Connecticut, United States

Site Status

Countries

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United States

References

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Sugarman DE, Poling J, Sofuoglu M. The safety of modafinil in combination with oral ∆9-tetrahydrocannabinol in humans. Pharmacol Biochem Behav. 2011 Mar;98(1):94-100. doi: 10.1016/j.pbb.2010.12.013. Epub 2010 Dec 21.

Reference Type RESULT
PMID: 21176784 (View on PubMed)

Bosnjak Kuharic D, Markovic D, Brkovic T, Jeric Kegalj M, Rubic Z, Vuica Vukasovic A, Jeroncic A, Puljak L. Cannabinoids for the treatment of dementia. Cochrane Database Syst Rev. 2021 Sep 17;9(9):CD012820. doi: 10.1002/14651858.CD012820.pub2.

Reference Type DERIVED
PMID: 34532852 (View on PubMed)

Other Identifiers

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MIRECC 00000000

Identifier Type: REGISTRY

Identifier Source: secondary_id

P50DA009241

Identifier Type: NIH

Identifier Source: secondary_id

View Link

0702002357

Identifier Type: -

Identifier Source: org_study_id

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