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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT04860089
Other study ID # 2019-10394
Secondary ID GRANT132671471K2
Status Withdrawn
Phase
First received
Last updated
Start date August 2022
Est. completion date June 30, 2025

Study information

Verified date September 2022
Source Montefiore Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date June 30, 2025
Est. primary completion date December 12, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Locations

Country Name City State
n/a

Sponsors (5)

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

Outcome

Type Measure Description Time frame Safety issue
Primary Pain severity 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. 14 weeks
Secondary Circulating levels of inflammatory cytokines 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 14 weeks
Secondary Antiretroviral adherence Measured at 0 and 14 weeks Visual Analog Scale [VAS] (0-100) with higher number indicating better adherence. 14 weeks
Secondary HIV Viral load suppression HIV viral load measured at two time points (baseline and 14 weeks; copies/mL) 14 weeks
Secondary Depression Measured at 0 and 14 weeks with the Patient Health Questionnaire- 9 [PHQ-9] (0-27) with higher score indicating worse depression 14 weeks
Secondary Anxiety Measured at 0 and 14 weeks with the Generalized Anxiety Disorder-7 [GAD-7] (0-21) with higher score indicating worse anxiety 14 weeks
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