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USClinicalTrials.govClinical trialNot applicableRecruiting

Buprenorphine Implementation at Syringe Service Programs to Reduce Overdoses

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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