A Randomized Controlled Trial Examining Extended-Release Injectable Buprenorphine in those who use High Potency Synthetic Opioids
A Clinical Trial Comparing Buprenorphine Medications for people who use Fentanyl and/or other High Potency Synthetic Opioid Use
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
Additional Study Information: 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
Do You Qualify?
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
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You may be eligible for this study

Place Holder




For more information, please contact:
Rachel Luba
rrl2117@cumc.columbia.edu
646-774-8189