Can The Bridge Transition Opiate Use Disorder Patients in Stable Recovery

Status Withdrawn

Clinical Trial Summary

Clinical Trial 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 Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03762798
Study type	Interventional
Source	The Cleveland Clinic
Contact
Status	Withdrawn
Phase	N/A
Start date	November 19, 2018
Completion date	December 1, 2020

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

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms