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NCT Number: NCT05339256

Sublingual Buprenorphine Through Telemedicine vs In-Person Care as Usual

This study will compare in-person induction and maintenance dosing of sublingual buprenorphine to induction and maintenance dosing of sublingual buprenorphine through comprehensive telehealth sessions and telehealth medication for opioid use disorder (MOUD).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

About this study

The study is a 12-week, randomized, active-control, open-label, early phase II effectiveness trial of telemedicine treatment using sublingual buprenorphine as compared to in person clinic treatment with sublingual buprenorphine for outpatients seeking treatment for opioid use disorder (OUD). This telehealth protocol serves as a model of the integration of evidence-based practices in medication for opioid use disorder (MOUD) and could be used by non addiction specialists at scale. The primary outcome will be time to dropout. Participants will have daily study visits (either in person or remote) during the initial buprenorphine induction week and then twice per week during the maintenance phase (either in person or remote) over the 12-week trial. Remote visits will be conducted using the HIPAA-compliant technology, FaceTime and/or Webex.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • meet DSM-5 criteria for OUD
  • Voluntarily seeking buprenorphine treatment for OUD
  • Able to provide informed consent and comply with study procedures

Exclusion criteria

  • Meeting DSM-5 criteria for substance use disorder other than opioid as the primary diagnosis that would compromise safety of participation in the trial as determined by the study physician, such as an alcohol or sedative hypnotic use disorder that requires detoxification
  • Having a comorbid psychiatric diagnosis that might interfere with participation or make participation hazardous, such as a psychotic disorder including schizophrenia or schizoaffective disorder
  • Concurrent methadone, buprenorphine, or vivitrol maintenance treatment
  • Known history of allergy, intolerance, or hypersensitivity to candidate medication (buprenorphine)
  • Pregnancy, lactation, or failure to use adequate contraceptive methods in female patients
  • Unstable medical conditions, such as severe hepatic, renal, or cardiovascular disease, which might make participation
  • Current or recent history history of significant violent or suicidal behavior or risk for suicide or homicide
  • Legally mandated to substance use disorder treatment.

Treatment and study plan

Buprenorphine SL

Drug

Up to 24 mg per day

Telehealth

Other

Telehealth MOUD, utilizing a standardized protocol for each healthcare provider session

In-person treatment as usual

Other

in-person induction and maintenance dosing of sublingual buprenorphine, or MOUD as usual.

Primary outcomes

  1. Time to drop out

    Time frame: 12 weeks

    Comparing time to drop out between the treatment arms

Study contacts

Contact information is provided by the study sponsor or research team.

Christina Brezing, MD

CONTACT

[email protected]

646-774-6132

Elizabeth Martinez

CONTACT

646-774-8181

Sponsors and collaborators

Lead sponsor

New York State Psychiatric Institute

Other

Collaborators

  • National Institute on Drug Abuse (NIDA)

Registry information

Official study title

A Randomized, Controlled Trial of Sublingual Buprenorphine Through Telemedicine vs In-Person Care as Usual in the Treatment of Opioid Use Disorder

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Apr 21, 2022
Registry last updated
Apr 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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