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Clinical trialNCT07631598RecruitingInterventional

Buprenorphine Implementation at Syringe Service Programs to Reduce Overdoses

SponsorMontefiore Medical CenterEnrollment512Opioid Use DisorderOpioid Use Disorder, ModerateOpioid Use Disorder, Severe
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

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.

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

8 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Community Health Project Los Angeles (chpla)

    Los Angeles, California, United States

    Amanda Cowan, MSc
    Recruiting
  • Hips

    Washington D.C., District of Columbia, United States

    Recruiting
  • Carpbr/be Safe Syringe Program

    Baton Rouge, Louisiana, United States

    Gjvar Payne
    Recruiting
  • Harm Reduction Sisters

    Duluth, Minnesota, United States

    Sue Purchase
    Recruiting
  • Alianza of New Mexico

    Roswell, New Mexico, United States

    Ryan Nix
    Recruiting
  • Hiv Alliance

    Grants Pass, Oregon, United States

    Harmony BeckettMichaela Starr O'Leary
    Recruiting
  • Challenges, Inc/prisma Health

    Greenville, South Carolina, United States

    Alain Litwin, MDMarc Burrows, MSW, LMSW, CPSS
    Recruiting
  • Vivent Health

    Milwaukee, Wisconsin, United States

    Mikaela Becker
    Recruiting

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
17 Aug 2026
Primary completion
29 Feb 2028
Completion
30 Jun 2028
Last update posted
21 Aug 2026
Registered enrollment
512
Registry id
NCT07631598

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.