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Open-Label, Safety Study of Lofexidine — NU LEAF  

Opioid Withdrawal Clinical Trial

Official title:
A Phase 3, Open-Label, Safety Study of Lofexidine

Clinical Trial Summary

The purpose of this Phase 3 open-label treatment study is to evaluate the safety and effectiveness of lofexidine at a clinically relevant dose to alleviate symptoms of acute withdrawal from any opioid, including methadone and buprenorphine. This study will take place in a variety of clinical scenarios, both in-clinic and outpatient settings.

Clinical Trial Description

Eligible subjects (person seeking treatment for partial or total opioid withdrawal) enrolled in this study are required to take lofexidine for a minimum of 7 days. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02363998
Study type Interventional
Source USWM, LLC (dba US WorldMeds)
Contact
Status Completed
Phase Phase 3
Start date February 2015
Completion date October 2015
View Details
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