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Study of Wafermine™ for Post-bunionectomy or Abdominoplasty Pain

Acute Pain Clinical Trial

Official title:
A Phase 2, Multiple-Dose Study of The Efficacy and Safety of Wafermine™ (Sublingual Ketamine) in Participants Experiencing Acute Post-Operative Bunionectomy or Abdominoplasty Pain

Clinical Trial Summary

This study evaluates the safety and effectiveness of Wafermine™ for post-bunionectomy or post-abdominoplasty pain over a 24 hours period. For subjects undergoing bunionectomy, 2 out of 3 subjects will receive Wafermine™ and 1 out of 3 subjects will receive placebo. For subjects undergoing abdominoplasty, 3 out of 4 subjects will receive Wafermine™ and 1 out of 4 subjects will receive placebo.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03246971
Study type Interventional
Source iX Biopharma Ltd.
Contact
Status Completed
Phase Phase 2
Start date August 24, 2017
Completion date July 17, 2018
View Details
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