Can The Bridge Transition Opiate Use Disorder Patients in Stable Recovery From Buprenorphine to Naltrexone

Not Applicable

Withdrawn

• Conditions: Substance Use Disorders; Substance Abuse; Substance Dependence; Substance Use
• Interventions: Device: The Bridge

• Registration Number: NCT03762798
• Lead Sponsor: The Cleveland Clinic

Brief Summary

This is an open-label, single center study of The Bridge in patients with sustained remission of opiate dependence on established, low-dose MAT with buprenorphine. A fixed number of patients will be admitted to the study.

Detailed Description

This is an open-label, single center study of The Bridge in patients with sustained remission of opiate dependence on established, low-dose MAT with buprenorphine. A fixed number of patients will be admitted to the study.

After determination that the subject meets the inclusion criteria and does not meet any of the exclusion criteria for the study, the subject will receive the device which will be applied in the clinical office setting on an outpatient basis. Buprenorphine MAT will be stopped immediately and the subject will be followed on an outpatient basis to ensure the process has been successful. The subject will have the option to return to the office for a follow-up assessment in 1-4 days after device application. Seven to ten days after the last dose of buprenorphine, a urine sample will be collected for drug testing and a prescription for naltrexone will be provided. Then three visits on a roughly monthly basis will be scheduled. At each visit a urine sample for drug testing will be collected. After three follow-up visits are completed, if the drug testing demonstrates continued sobriety, the subject will be released from the study and may or may not continue treatment with naltrexone.

Study Timeline

• Study Start: 2018-11-19
• Study First Submitted: 2018-11-28
• Study First Submitted QC: 2018-12-03
• Study First Posted: 2018-12-04
• Primary Completion: 2020-10-25
• Study Completion: 2020-12-01
• Status Verified: 2021-09
• Last Update Submitted: 2021-09-17
• Last Update Posted: 2021-09-23

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

• Diagnosis of opiate use disorder, any severity
• Age range 18-99 years old
• Not pregnant or breastfeeding
• Able to understand and provide informed consent.
• Able to understand and speak the English language.
• At least one year of abstinence from drugs of abuse including, but not limited to, all opiates, cannabis, benzodiazepines, barbiturates, alcohol and cocaine.
• Use of nicotine is excluded from this criterion.
• Use of any prescribed, controlled substance, taken according to the prescribing instructions, for no more than seven consecutive days, at least three months prior to the subject's study enrollment, is excluded from this criterion.
• Taking dose of buprenorphine less than or equal to no more than 4 mg daily for at least three months prior to starting the study.
• In the case of Zubsolv rapid-dissolve tablets, equivalent daily dose maximum would be 2.9mg.
• In the case of Bunavail buccal film, equivalent daily dose maximum would be 2.1mg.
• At least one year of self-reported, established 12-step based recovery work, including
• Home group membership and regular attendance of two 12- step meetings per week
• Regular work with 12-step sponsor who can attest that the subject has worked through step nine of the twelve steps of Alcoholics Anonymous or a similar 12-step based mutual help organization.

Exclusion Criteria

• Exhibits active psychosis or suicide ideation or is otherwise psychiatrically unstable.
• Positive Utox2 Immunoassay, Quantitative Pain Panel Liquid Chromatography/Mass Spectroscopy, or Ethylglucuronide test for any nonprescribed substance or medication.
• Meets criteria for any other active substance use disorder except nicotine
• Allergic to naltrexone or has any condition of such nature and/or severity that would clinically contraindicate the prescribing of naltrexone.
• Any condition that contraindicates the use of NSS-2 including hemophilia, cardiac pacemakers and psoriasis vulgaris.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Treatment	The Bridge	All participants will receive the Bridge device.

Primary Outcome Measures

Name	Time	Method
Primary Objective	Three Months	Number of patients who complete three follow-up visits while taking naltrexone and produce entirely negative urine opiate screens during that period

Trial Locations

Locations (1)

Cleveland Clinic Lutheran Hospital; 🇺🇸 Cleveland, Ohio, United States