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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04385082
Other study ID # 19-000876
Secondary ID R01DA047296
Status Recruiting
Phase Phase 1
First received
Last updated
Start date July 8, 2021
Est. completion date June 30, 2026

Study information

Verified date May 2024
Source University of California, Los Angeles
Contact Ziva Cooper, PhD
Phone 310-206-9942
Email zcooper@mednet.ucla.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this research is to assess the impact of cannabis on the analgesic and abuse-related effects between men and women


Description:

The proposed study will compare smoked cannabis's dose-dependent, analgesic and abuse-related effects between men and women and variables that underlie these sex-dependent differences, including pharmacokinetics of THC.


Recruitment information / eligibility

Status Recruiting
Enrollment 160
Est. completion date June 30, 2026
Est. primary completion date June 30, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years to 55 Years
Eligibility Inclusion Criteria: - Male or non-pregnant female aged 21-55 years - Report use of cannabis an average of 1-7 days per week - Not currently seeking treatment for their cannabis use - Urine test positive for recent cannabis use for heavy users - No reported adverse effects with cannabis smoking in light users - Have a Body Mass Index from 18.5 - 34kg/m2. - Able to perform all study procedures - FEMALES: Currently practicing a non-hormonal effective form of birth control - FEMALES: Must be regularly cycling Exclusion Criteria: - Meeting DSM-V criteria for any substance use disorder other than nicotine, caffeine, or cannabis use disorder - Report using other illicit drugs in the prior 4 weeks - History or current evidence of severe psychiatric illness or medical condition judged by the study physician and PI to put the participant at greater risk of experiencing adverse events due to completion of study procedures, interfere with their ability to participate in the study, or their capacity to provide informed consent. - Current use of medical cannabis, prescription analgesics, or any medications that may affect study outcomes - Current pain - Insensitivity to the cold water stimulus of the Cold Pressor Test - FEMALES: using a hormonal contraceptive

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Active Cannabis
Smoked cannabis with THC
Placebo Cannabis
Placebo smoked cannabis (no THC)

Locations

Country Name City State
United States University of California, Los Angeles Los Angeles California

Sponsors (2)

Lead Sponsor Collaborator
University of California, Los Angeles National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Subject-rated drug effects Average and peak subjective ratings of drug effects associated with abuse liability as measured using visual analogue scales (VAS; 1-100mm). 5 hours
Primary Analgesia as measured using the Cold Pressor Test Peak and average pain threshold and tolerance assessed using the Cold Pressor Test 5 hours
Primary Pharmacokinetics of THC and metabolites Plasma levels of THC, 11-OH-THC, and THCCOOH 5 hours
Secondary Drug reinforcement using the cannabis self-administration task Average number of cannabis puffs self-administered as a function of cannabis strength and sex. For this task, up to three 'puffs' of cannabis may be chosen for self-administration during each session. 5 hours
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