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NCT00624715

Cannabinoid Receptor Function & Alcoholism

Completed Phase 1 Last updated 11 March 2022
What this trial tests

Phase 1 trial testing THC in Alcoholism in 29 participants. Completed in 22 June 2010.

Timeline
9 August 2007
Primary endpoint
22 June 2010
22 June 2010

Quick facts

Lead sponsorYale University
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingquadruple
Primary purposebasic science
Enrollment29
Start date9 August 2007
Primary completion22 June 2010
Estimated completion22 June 2010
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Yale University

Who can join

Adults 18 to 30, any sex, with Alcoholism. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study attempts to characterize the effects of tetrahydrocannabinol (THC). Tetrahydrocannabinol is the active ingredient of marijuana, cannabis, "ganja", or "pot". This study will involve healthy volunteers who 1) have no history of alcoholism in their family or 2) have a family history of alcoholism. This study looks at individuals with or without a family history of alcoholism to determine if there is a difference between the two groups in the response to THC.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of THC

Trials testing the same drug.

Other recruiting trials for Alcoholism

Currently open trials in the same condition.

Other Yale University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00624715.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing