MEMO-Medical Marijuana and Opioids Study

Sponsor
Albert Einstein College of Medicine (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT03268551
Collaborator
Fordham University (Other), Columbia University (Other), National Institute on Drug Abuse (NIDA) (NIH)
250
2
57.8
125
2.2

Study Details

Study Description

Brief Summary

The study will examine how medical cannabis use affects opioid analgesic use over time, with particular attention to THC/CBD content, HIV outcomes, and severe adverse events.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The overarching goal of the study is to understand how medical cannabis use affects opioid analgesic use over time, with particular attention to THC/CBD content, HIV outcomes, and adverse events. The study will include a cohort of 250 HIV+ and HIV- adults with (a) severe or chronic pain, (b) opioid analgesic use, and (c) new certification for medical cannabis. Over 18 months, participants will have 7 in-person visits every 3 months and 39 web-based questionnaires every 2 weeks. Data sources will include questionnaires; medical, pharmacy, and Prescription Monitoring Program records; and urine and blood samples. Over each 2-week time period (unit of analysis), the primary exposure measure will be number of days of medical cannabis use, and the primary outcome measure will be cumulative opioid analgesic dose. Qualitative interviews will also be conducted with a subgroup of 30 participants to explore perceptions of how medical cannabis use affects opioid analgesic use. Qualitative findings will help understand the reasons underlying the findings of the cohort study.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    250 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Does Medical Cannabis Reduce Opioid Analgesics in HIV+ and HIV- Adults With Pain?
    Actual Study Start Date :
    Sep 4, 2018
    Anticipated Primary Completion Date :
    Jun 30, 2023
    Anticipated Study Completion Date :
    Jun 30, 2023

    Outcome Measures

    Primary Outcome Measures

    1. Opioid analgesic use [Opioid analgesic use will be a cumulative dose of all opioid analgesics over each of the 39 2-week periods.]

      The primary outcome will combine measures of prescribed and illicit opioid analgesic use.

    Secondary Outcome Measures

    1. Alternative measures of opioid analgesic use [Alternative measures of opioid analgesic use will be measured over each of the 39 2-week periods.]

      Alternative measures of opioid analgesic use will include: number of days of all opioid analgesic use, mean daily dose of all opioid analgesics, cumulative dose of prescribed (only) opioid analgesics, number of days of prescribed (only) opioid analgesic use, and mean daily dose of prescribed (only) opioid analgesic use.

    2. HIV viral load [HIV outcomes will be measured seven times every 3 months from baseline through 18 months.]

      HIV viral load will be measured in copies/ml from blood samples collected during the study.

    3. CD4 count [CD4 count will be measured seven times every 6 months from baseline through 18 months..]

      CD4 count will be measured in cells/mm3 from blood samples collected during the study.

    4. HIV antiretroviral adherence [HIV antiretroviral adherence will be measured seven times every 3 months from baseline through 18 months..]

      HIV antiretroviral adherence will be a composite measure from self-reported questionnaires and pharmacy records.

    5. HIV risk behaviors [HIV risk behaviors will be measured seven times every 3 months from baseline through 18 months..]

      HIV risk behaviors will be a composite measure from self-reported questionnaires.

    6. Cannabis use disorder [Cannabis use disorder will be measured three times every 6 months.]

      Cannabis use disorder will be measured using standardized instruments.

    7. Illicit drug use [Illicit drug use will be measured seven times every 3 months from baseline through 18 months..]

      Illicit drug use will be measured using standardized surveys and urine toxicology testing.

    8. Diversion of medical cannabis [Diversion will be measured seven times every 3 months from baseline through 18 months..]

      Diversion will be measured using standardized surveys.

    9. Non-fatal overdose [Non-fatal overdose will be measured seven times every 3 months from baseline through 18 months..]

      Non-fatal overdose will be measured using standardized surveys.

    10. Death [Death will be measured 18 months after enrollment.]

      Death will be ascertained from the National Death Index

    11. Accidents/Injuries [Accident/Injuries will be measured seven times every 3 months from baseline through 18 months..]

      Accidents/Injuries will be measured using standardized survey instruments

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • At least 18 years of age

    • English or Spanish fluency

    • New certification for medical cannabis within 90 days

    • No medical cannabis use in the 6 months prior to certification

    • Medical cannabis qualifying complication of "chronic or severe pain"

    • Use of prescribed or illicit opioid analgesics within 30 days

    Exclusion Criteria:
    • Inability to provide informed consent

    • Inability to complete study visits over 18 months

    • Qualifying conditions for medical cannabis in NY that are likely to cause unique pain syndromes (cancer, epilepsy, multiple sclerosis, spinal cord injury, amyotrophic lateral sclerosis, Parkinson's disease, inflammatory bowel disease, Hungtington's disease)

    • Terminal illness

    • Current or prior psychotic disorder

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Montefiore Health System Bronx New York United States 10451
    2 Vireo Health White Plains New York United States 10601

    Sponsors and Collaborators

    • Albert Einstein College of Medicine
    • Fordham University
    • Columbia University
    • National Institute on Drug Abuse (NIDA)

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    Albert Einstein College of Medicine
    ClinicalTrials.gov Identifier:
    NCT03268551
    Other Study ID Numbers:
    • 2017-7857
    • 1R01DA044171-01A1
    First Posted:
    Aug 31, 2017
    Last Update Posted:
    Aug 3, 2022
    Last Verified:
    Aug 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 3, 2022