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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


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

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