Dronabinol Interactions With Cognitive Enhancing Drug in Humans
NCT ID: NCT00842985
Last Updated: 2017-05-30
Study Results
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View full resultsBasic Information
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COMPLETED
EARLY_PHASE1
53 participants
INTERVENTIONAL
2008-09-30
2009-10-31
Brief Summary
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We hypothesize that modafinil treatment will decrease ratings of drug liking and improve cognitive measures, especially episodic memory.
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Detailed Description
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Currently this study complete and has been published.
Conditions
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Study Design
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SEQUENTIAL
TREATMENT
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.
drug condition
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
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* 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 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.
18 Years
55 Years
ALL
No
Sponsors
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VA Office of Research and Development
FED
National Institute on Drug Abuse (NIDA)
NIH
Yale University
OTHER
Responsible Party
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Mehmet Sofuoglu
M.D., Ph.D.
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
Countries
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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.
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.
Other Identifiers
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MIRECC 00000000
Identifier Type: REGISTRY
Identifier Source: secondary_id
0702002357
Identifier Type: -
Identifier Source: org_study_id
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