This is an investigation involving the use of a long-acting, injectable form (depot) of naltrexone as a treatment for persons who have a history of opioid dependence, with up to 40 on parole/probation and 20 non-parolees. The test is a pilot study of up to 60 subjects treated with 6 months of depot naltrexone plus Psychosocial Treatment .
This is a two phase study. Phase 1 is complete and phase 2 is not yet recruiting.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
61
228mg of injectable naltrexone
University of Pennsylvania
Philadelphia, Pennsylvania, United States
UDS results
Time frame: 6 months
Treatment completion
Time frame: 6 months
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