Last updated: February 15, 2024
Sponsor: Glenn-Milo Santos
Overall Status: Active - Not Recruiting
Phase
2
Condition
Stimulant Use Disorder
Treatment
Naltrexone Hydrochloride
Ecological Momentary Intervention
Placebo
Clinical Study ID
NCT04791969
20-32912
DA053171-01A1
Ages 18-70 Male Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- cisgender male (male gender and sex assigned at birth)
- age 18-70 years* (naltrexone's tolerability and safety has been demonstrated amongolder adults up to age 70)
- self-reported condomless anal sex with men or missing Pre-Exposure Prophylaxis orantiretroviral therapy doses due to meth use in the prior three months while under theinfluence of meth
- self-reported meth use at least weekly
- mild, moderate or severe meth use disorder
- positive meth sample via sweat patch or urine testing during screening
- interested in reducing meth use
- no current acute illness requiring prolonged medical care
- no chronic illness that is likely to progress clinically during trial
- able and willing to provide informed consent and adhere to visit schedule
- current CD4 count ≥ 200 cells/mm3; or CD4 count of 100-199 cells/mm3 and HIV viralload < 200 copies/mL (if living with HIV)
- baseline complete blood count, total protein, albumin, glucose, alkaline phosphatase,creatinine, blood urea nitrogen test, and electrolytes without clinically significantabnormalities as determined by study clinician in conjunction with symptoms, physicalexam, and medical history
Exclusion
Exclusion Criteria:
- any psychiatric (e.g., depression with suicidal ideation) or medical condition thatwould preclude safe participation
- known allergy or prior adverse reaction to naltrexone
- current use of any opioids or a known medical condition which currently requires ormay likely require opioid analgesics
- opioid-positive urine test at screen/enrollment visits (naltrexone can induce opioidwithdrawal)
- moderate or severe liver disease (aspartate aminotransferase test, alanineaminotransferase test, or total bilirubin > 3 times upper limit of normal)
- impaired renal function (creatinine clearance < 60 ml/min)
- currently participating in another intervention research study with potential overlap
- severe alcohol use disorder as determined by structured clinical interview for DSM-5criteria
- any condition that, in the PI and/or study clinician's judgment interferes with safeparticipation or adherence to study procedures
Study Design
Total Participants: 54
Treatment Group(s): 3
Primary Treatment: Naltrexone Hydrochloride
Phase: 2
Study Start date:
December 14, 2021
Estimated Completion Date:
July 01, 2024
Study Description
Connect with a study center
San Francisco Department of Public Health
San Francisco, California 94102
United StatesSite Not Available
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