A Randomized Controlled Trial Examining Extended-Release Injectable Buprenorphine in those who use High Potency Synthetic Opioids
Sponsor: |
National Institute on Drug Abuse |
Enrolling: |
Male and Female Patients |
Study Length: |
12 Weeks |
Clinic Visits: |
12 |
IRB Number: |
AAAV2503 |
U.S. Govt. ID: |
NCT06726200 |
Contact: |
Rachel Luba: 646-774-8189 / rrl2117@cumc.columbia.edu |
Columbia University Medical Center is recruiting individuals ages 18-65 who are seeking treatment for opioid use disorder to participate in a research treatment study. For your participation, you'll receive treatment with buprenorphine (either sublingual or injectable) at no cost. Participants will complete an overnight inpatient stay to start buprenorphine and then return for follow up visits. Participants will be compensated up to $540 for completion of all screening and follow up visits.
Investigator
Rachel Luba, PhD
Are you voluntarily seeking treatment for opioid use? |
Yes |
No |
Are you currently pregnant or attempting to become pregnant? |
Yes |
No |
Are you currently using opioids like fentanyl, heroin, or other high potency synthetic opioids? |
Yes |
No |
Are you willing to take buprenorphine? |
Yes |
No |