PITCH-E: Pain, Inflammation, and Cannabis in HIV

Sponsor
Montefiore Medical Center (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04860089
Collaborator
National Institute on Drug Abuse (NIDA) (NIH), University of Colorado, Boulder (Other), University of Pittsburgh (Other), Vireo Health (Other)
100
35

Study Details

Study Description

Brief Summary

This study will examine how medical cannabis use affects neuropathic pain, inflammation and adverse events in people living with HIV (PLWH) with neuropathic pain. We will study how varying ratios of THC and CBD in medical cannabis impact neuropathic pain, inflammation and adverse events.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    This study will examine how medical cannabis use affects neuropathic pain in PLWH with neuropathic pain. We will enroll adults with HIV who have a) neuropathic pain, b) are actively certified for medical cannabis, and c) intend to have soft gel capsule products dispensed at Vireo (medical cannabis dispensary) (including a high THC:low CBD product, an equal THC:CBD product, and a low THC:high CBD product). Over 14 weeks, data sources will include questionnaires, blood samples, urine samples; medical, pharmacy, and Prescription Monitoring Program (PMP) records. The primary independent variable will be type of medical cannabis product dispensed at dispensary, and the primary outcome will be self-reported pain.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    100 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    The Impact of Medical Cannabis on Pain and Inflammation in People Living With HIV
    Anticipated Study Start Date :
    Aug 1, 2022
    Anticipated Primary Completion Date :
    Dec 12, 2023
    Anticipated Study Completion Date :
    Jun 30, 2025

    Outcome Measures

    Primary Outcome Measures

    1. Pain severity [14 weeks]

      self-reported pain severity measured via the Brief Pain Interference (BPI) severity scale (1-10) with higher score indicating worse pain. Measured weekly with web- or phone-based questionnaire.

    Secondary Outcome Measures

    1. Circulating levels of inflammatory cytokines [14 weeks]

      Tests levels of recent inflammation (panel of inflammatory markers) at two time points before starting medical cannabis and 14 weeks after starting medical cannabis. Reported in pg/mL

    2. Antiretroviral adherence [14 weeks]

      Measured at 0 and 14 weeks Visual Analog Scale [VAS] (0-100) with higher number indicating better adherence.

    3. HIV Viral load suppression [14 weeks]

      HIV viral load measured at two time points (baseline and 14 weeks; copies/mL)

    4. Depression [14 weeks]

      Measured at 0 and 14 weeks with the Patient Health Questionnaire- 9 [PHQ-9] (0-27) with higher score indicating worse depression

    5. Anxiety [14 weeks]

      Measured at 0 and 14 weeks with the Generalized Anxiety Disorder-7 [GAD-7] (0-21) with higher score indicating worse anxiety

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • = 18 years old

    • Diagnosis of HIV

    • Fluency in English

    • Active certification for medical cannabis

    • No medical cannabis dispensed or used within the previous 30 days

    • Intends to purchase soft-gel capsule medical cannabis at Vireo

    • ICD-10 diagnosis code for neuropathic pain, OR

    • Neuropathic pain in problem list of electronic medical record, OR

    • Neuropathic pain questionnaire-short form>0

    Exclusion Criteria:
    • Inability to provide informed consent

    • Inability to complete 14 weeks of study visits

    • Medical cannabis use within 30 days prior to enrollment

    • Unique pain symptoms (e.g. multiple sclerosis, rheumatoid arthritis)

    • Terminal illness

    • Current or prior psychotic disorder

    • Street cannabis, opioid, cocaine, or benzodiazepine use in the past 30 days

    • Dispensed opioids of benzodiazepines within 60 days

    • Non-steroidal anti-inflammatory use within 7 days prior to enrollment

    • Steroid use within the past 14 days with duration of therapy >=21 days

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Montefiore Medical Center
    • National Institute on Drug Abuse (NIDA)
    • University of Colorado, Boulder
    • University of Pittsburgh
    • Vireo Health

    Investigators

    • Principal Investigator: Deepika E Slawek, MD, MPH, MS, Montefiore Medical Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Deepika Slawek, Assistant Professor of Medicine, Montefiore Medical Center
    ClinicalTrials.gov Identifier:
    NCT04860089
    Other Study ID Numbers:
    • 2019-10394
    • GRANT13267147
    • 1K23DA053997-01A1
    First Posted:
    Apr 26, 2021
    Last Update Posted:
    Jul 25, 2022
    Last Verified:
    Jul 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    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 Jul 25, 2022