ACTIVE_NOT_RECRUITING

Analgesic and Subjective Effects of Terpenes

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of this research is to assess the analgesic and subjective effects of terpenes administered alone and in combination of THC.

Official Title

Analgesic and Subjective Effects of Terpenes Administered Alone and in Combination With THC

Quick Facts

Study Start:2021-12-15
Study Completion:2026-04-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT04451863

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:21 Years to 55 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Male or non-pregnant female aged 21-55 years
  2. * Report non-medical use of cannabis 1-7 days per week over the 1 month prior to screening
  3. * Not currently seeking treatment for cannabis use
  4. * Urine test positive for recent cannabis use
  5. * Have a Body Mass Index from 18.5 - 34kg/m2.
  6. * Able to perform all study procedures
  7. * Must be using a contraceptive method (hormonal or barrier methods)
  1. * Meeting DSM-V criteria for any substance use disorder other than nicotine, caffeine, or mild CUD
  2. * Report using other illicit drugs in the prior 4 weeks
  3. * • If medical history, physical and psychiatric examination, or laboratory tests performed during the screening process not within the normal range and / or reveal any significant illness (e.g., hypertension) as judged by the study physician and to put the participant at greater risk of experiencing adverse events due to completion of study procedures.
  4. * Current licit use of cannabis primarily for medical purposes, prescription analgesics, or any medications that may affect study outcomes
  5. * Current pain
  6. * Pregnancy is exclusionary due to the possible effects of the study medication on fetal development.
  7. * History of an allergic reaction or adverse reaction to cannabis is exclusionary.
  8. * History of respiratory illness or current respiratory illness
  9. * History of seizure disorder or current seizure disorder
  10. * Insensitivity to the cold water stimulus of the Cold Pressor Test
  11. * Currently enrolled in another research protocol
  12. * Current major Axis 1 disorders (mood, anxiety, or psychotic disorder)
  13. * Not using a contraceptive method (hormonal or barrier methods)
  14. * The evaluating physician reviews all medical assessments along with medical history. Any disorders that might make cannabis administration hazardous are exclusionary.

Contacts and Locations

Principal Investigator

Ziva Cooper, PhD
PRINCIPAL_INVESTIGATOR
University of California, Los Angeles

Study Locations (Sites)

University of California, Los Angeles
Los Angeles, California, 90095
United States

Collaborators and Investigators

Sponsor: University of California, Los Angeles

  • Ziva Cooper, PhD, PRINCIPAL_INVESTIGATOR, University of California, Los Angeles

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2021-12-15
Study Completion Date2026-04-30

Study Record Updates

Study Start Date2021-12-15
Study Completion Date2026-04-30

Terms related to this study

Keywords Provided by Researchers

  • Cannabis
  • Analgesia
  • Pain
  • THC
  • Terpenes

Additional Relevant MeSH Terms

  • Pain
  • Abuse, Drug