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A Study of Cebranopadol for the Treatment of Acute Pain After Bunionectomy — ALLEVIATE2  

Acute Pain Clinical Trial

Official title:
A Multicenter, Randomized, Double-Blind, Placebo- and Active-Controlled Study to Evaluate the Efficacy and Safety of Cebranopadol for the Treatment of Moderate to Severe Acute Pain After Primary Unilateral Bunionectomy

Clinical Trial Summary

The purpose of this study is to evaluate the efficacy and safety of Cebranopadol for acute pain after a bunionectomy.

Clinical Trial Description

This study is a Phase 3, multicenter, randomized, double-blind, placebo- and active-controlled parallel-group study to evaluate the efficacy and safety of cebranopadol in the treatment of postoperative pain following primary unilateral bunionectomy with first metatarsal osteotomy. The study will be conducted in 3 phases: Screening, Treatment, and Follow-up. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06423703
Study type Interventional
Source Tris Pharma, Inc.
Contact Antonio Pardo, MD
Phone 732-823-4755
Email clinicalaffairs@trispharma.com
Status Not yet recruiting
Phase Phase 3
Start date May 2024
Completion date December 2024
View Details
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