Low-dose Buprenorphine Initiation for Opioid Use Disorder

Status Recruiting

Clinical Trial Summary

The purpose of this study is to test whether low-dose buprenorphine initiation for treatment of opioid use disorder is safe and effective.

Clinical Trial Description

After being informed about the study and potential risks, all participants will be given written informed consent. Eligible participants will be randomized in a 1:1 ratio to an 8-day low-dose buprenorphine initiation protocol or treatment as usual, and conduct study visits at baseline and weeks 2 and 4. The investigators will also provide participants with mobile phones to collect real-time data on withdrawal, anxiety, craving and substance use through electronic Ecological Momentary Assessment (EMA) technology. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05450718
Study type	Interventional
Source	Montefiore Medical Center
Contact	Benjamin T Hayes, MD, MS, MPH
Phone	4156700850
Email	bhayes@montefiore.org
Status	Recruiting
Phase	Phase 4
Start date	June 20, 2024
Completion date	July 30, 2027

View Details

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