Lofexidine for Adults Undergoing Lumbar Spine Surgery

Status Completed

Clinical Trial Summary

The primary objective is to investigate the effects of lofexidine in adults undergoing opioid tapering prior to elective lumbar spine surgery.

Clinical Trial Description

In this clinical trial, an open label design will be used to facilitate opioid tapering during a 12-day period prior to elective spine surgery. The primary outcome measure of this study is the number of patients who achieve a 50% reduction in daily opioid dose at day 12. ;

Study Design

Related Conditions & MeSH terms

Opioid Withdrawal

Clinical Trial Details

NCT number	NCT04126083
Study type	Interventional
Source	Mayo Clinic
Contact
Status	Completed
Phase	Phase 4
Start date	September 1, 2019
Completion date	April 15, 2021

View Details

See also
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