USClinicalTrials.govClinical trialNot applicableRecruiting
Buprenorphine Implementation at Syringe Service Programs to Reduce Overdoses
Official record
- Identifier
NCT07631598- Recruiting locations
country
United States- Interventions studied
- Standard of Care ReferralLow Threshold Buprenorphine
- Lead sponsor
- Montefiore Medical Center
- Target enrolment
- 512 participants
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Status
- Recruiting
- First posted
- Jun 8, 2026
- Last updated on the registry
- Oct 1, 2026
- Age
- 18 Years
- Sex
- ALL
- Study contact
- The official record lists a study contact. Contact details are published there and are intentionally not copied to this page.
- Eligibility criteria
Reproduced verbatim from the official record. Eligibility is decided by the study team, never by this page.
Inclusion Criteria: 1. ≥ 18 years old; 2. Meet DSM-5 criteria for moderate or severe OUD; 3. Interest in receiving buprenorphine treatment; 4. Speaks English or Spanish; 5. Currently an SSP client at the time of enrollment; 6. Ability to provide informed consent. Exclusion Criteria: 1. Current use of prescribed opioid agonist treatment, as assessed by self-report, at the time of enrollment; 2. Unstable mental health or medical condition that requires an immediate clinical evaluation or higher level of care; 3. Allergy to buprenorphine; 4. Currently detained in jail, prison, residential substance use treatment facility, or other overnight facility as required by court of law. or have pending legal action that could prevent participation on study activities.
- Indexed under
- Lymphoma