Optimizing Retention, Duration and Discontinuation Strategies for Opioid Use Disorder Pharmacotherapy (RDD)

Description

This is a two phase study investigating combinations of pharmacological and behavioral interventions to optimize the treatment of Opioid Use Disorder (OUD). The Retention Phase will assess strategies for improving retention on buprenorphine (BUP) and extended-release injectable naltrexone (XR-NTX). The Discontinuation Phase will assess which approaches are most likely to lead to long-term success (absence of relapse), and what characteristics of participants distinguish those who can safely discontinue Medications for Opioid Use Disorder (MOUD) from those who remain at risk of relapse and should not discontinue.

Conditions

Opioid Use Disorder (OUD)

Study Overview

Study Details

Study overview

This is a two phase study investigating combinations of pharmacological and behavioral interventions to optimize the treatment of Opioid Use Disorder (OUD). The Retention Phase will assess strategies for improving retention on buprenorphine (BUP) and extended-release injectable naltrexone (XR-NTX). The Discontinuation Phase will assess which approaches are most likely to lead to long-term success (absence of relapse), and what characteristics of participants distinguish those who can safely discontinue Medications for Opioid Use Disorder (MOUD) from those who remain at risk of relapse and should not discontinue.

NIDA-CTN-0100: Optimizing Retention, Duration and Discontinuation Strategies for Opioid Use Disorder Pharmacotherapy (RDD)

Optimizing Retention, Duration and Discontinuation Strategies for Opioid Use Disorder Pharmacotherapy (RDD)

Condition
Opioid Use Disorder (OUD)
Intervention / Treatment

-

Contacts and Locations

Little Rock

University of Arkansas for Medical Sciences (UAMS) / Center for Addiction Services and Treatment (CAST), Little Rock, Arkansas, United States, 72205

Tarzana

Tarzana Treatment Centers, Inc., Tarzana, California, United States, 91356

Bridgeport

Liberation Programs, Inc., Bridgeport, Connecticut, United States, 06610

Clearwater

Operation PAR, Clearwater, Florida, United States, 33760

Jacksonville

Gateway Community Services, Jacksonville, Florida, United States, 32204

Orlando

Aspire Health Partners, Orlando, Florida, United States, 32806

Baltimore

Mountain Manor / Maryland Treatment Centers, Baltimore, Maryland, United States, 21229

Belmont

McLean Hospital, Belmont, Massachusetts, United States, 02478

Fall River

Stanley Street Treatment and Resources, Inc., Fall River, Massachusetts, United States, 02720

Newton

Square Medical Group, LLC, Newton, Massachusetts, United States, 02458

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

    Ages Eligible for Study

    18 Years to

    Sexes Eligible for Study

    ALL

    Accepts Healthy Volunteers

    No

    Collaborators and Investigators

    NYU Langone Health,

    Edward V Nunes, MD, PRINCIPAL_INVESTIGATOR, New York State Psychiatric Institute/Columbia University Irving Medical Center

    John Rotrosen, MD, PRINCIPAL_INVESTIGATOR, NYU Grossman School of Medicine

    Roger Weiss, MD, PRINCIPAL_INVESTIGATOR, Harvard Medical School/McLean Hospital

    Study Record Dates

    2026-12-30