Phase
Condition
Stimulant Use Disorder
Treatment
Naltrexone Hydrochloride
Ecological Momentary Intervention
Placebo
Clinical Study ID
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 underthe influence 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, alkalinephosphatase, creatinine, blood urea nitrogen test, and electrolytes withoutclinically significant abnormalities as determined by study clinician in conjunctionwith symptoms, physical exam, 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 potentialoverlap
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
Study Description
Connect with a study center
San Francisco Department of Public Health
San Francisco, California 94102
United StatesSite Not Available
San Francisco Department of Public Health
San Francisco 5391959, California 5332921 94102
United StatesSite Not Available

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