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NCT07631598 · ClinicalTrials.gov registry record · NA
Buprenorphine Implementation at Syringe Service Programs to Reduce Overdoses
A NA study, sponsored by Montefiore Medical Center.
- Not yet
- Registry status
- NA
- Development phase
- 512
- Enrollment target
NCT07631598: Clinical Trial NA study, sponsored by Montefiore Medical Center.
NCT07631598 is a NA study that has not yet begun recruiting, run by Montefiore Medical Center. The registered enrollment target is 512 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (64% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07631598, a NA study, has not yet begun recruiting, sponsored by Montefiore Medical Center.
- NOT YET RECRUITING
- Registry status
- NA
- Development phase
- 512 participants
- Enrollment target
Study Summary
This study is testing whether offering buprenorphine treatment directly at syringe service programs (SSPs) helps more people start and stay in treatment for opioid use disorder (OUD) than referring them to community buprenorphine treatment providers. Buprenorphine is a medication that helps reduce opioid cravings and withdrawal symptoms. The study compares two ways of connecting people to treatment: Referral to a community treatment provider (usual care before the new program begins). Onsite, low-threshold buprenorphine treatment at the SSP, which allows participants to start medication quickly and without having to establish care at another provider. Participants will be adults who have opioid use disorder and are SSP clients. Each SSP will begin offering the new onsite buprenorphine program at different times during the study. Researchers will collect information before and after the new program begins to see how it affects treatment engagement and health outcomes. The study will also examine how easy or difficult it is for SSPs to start and run the new program, how acceptable it is to staff and participants, and whether it is cost-effective. The overall goal is to find better ways to expand access to life-saving opioid treatment in community-based settings.
Primary Outcome
Buprenorphine (BUP) treatment retention will be defined as having an active buprenorphine prescription between baseline and 1-month and between the 1-month (days 1-30) and 3-month (days 31-90) time points. Participants will be asked to provide evidence of BUP prescriptions at study visits (i.e., confirmed prescriptions). If a participant receives a second BUP prescription before the 1-month follow-up and the number of days dispensed covers dates after day 30 (i.e., carries over into the 31-90 da
Interventions
- OTHER Standard of Care Referral
- BEHAVIORAL Low Threshold Buprenorphine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 512 participants |
| Start Date | 2026-08-10 |
| Est. Completion | 2028-06 |
| Phase | NA |
What is known before NCT07631598 opens enrollment
NCT07631598 is an interventional study that assigns participants to a tested intervention. The registered 512 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (64% lower).
The record links to 0 conditions, and to 2 interventions - of which Standard of Care Referral is the first listed.
NCT07631598 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT07631598 about?
NCT07631598 is a clinical study titled "Buprenorphine Implementation at Syringe Service Programs to Reduce Overdoses". This study is testing whether offering buprenorphine treatment directly at syringe service programs (SSPs) helps more people start and stay in treatment for opioid use disorder (OUD) than referring them to community buprenorphine treatment providers. Buprenorphine is a medication that helps reduce o...
What is the current status of trial NCT07631598?
This trial is currently not yet recruiting. It is a NA study. The enrollment target is 512 participants. The study started on 2026-08-10. Estimated completion is 2028-06.
What interventions are being tested in trial NCT07631598?
The interventions under investigation include: Standard of Care Referral (OTHER), Low Threshold Buprenorphine (BEHAVIORAL).
Who is sponsoring clinical trial NCT07631598?
This trial is sponsored by Montefiore Medical Center, which has 345 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT07631598's enrollment target sits among peer trials
512 192nd of 2000 higher than 1,809 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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