Condition: Opioid Use Disorder · Sponsor: Pouya Azar
The goal of this clinical study is to evaluate a new treatment approach called symptom inhibited naloxone induction (SINI) for people with opioid use disorder. In this study, participants will receive small doses of intravenous (IV) naloxone at intervals until they feel mild opioid withdrawal symptoms. At this point, they will be given buprenorphine/naloxone under the tongue to help with the withdrawal symptoms. One hour after, they will receive a injection of long acting buprenorphine under the skin if they choose to. The main questions this study aims to answer are: Is it feasible to use the SINI protocol in inpatient and outpatient settings? Is the SINI protocol safe and tolerable for individuals with opioid use disorder?
This description comes directly from the study's public registry record.
James Wong, MSc · (604) 875-5823 · james.wong@vch.ca
Always discuss trial participation with your own doctor first.
| Hope to Health Research & Innovation Centre | Vancouver, British Columbia, Canada | Not Yet Recruiting |
| Vancouver General Hospital | Vancouver, British Columbia, Canada | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07439549