Study of Wafermine™ for Post-bunionectomy or Abdominoplasty Pain

Status Completed

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

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