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Controlled Study to Assess the Efficacy and Safety of S-Ibuprofen Topical Gel 5% (AP0302) in the Treatment of DOMS

Pain, Acute Clinical Trial

Official title:
A Randomized, Double-Blind,Vehicle-Controlled Study to Determine the Efficacy and Safety of AP0302 in the Treatment of Delayed Onset Muscle Soreness (DOMS)

Clinical Trial Summary

Phase 2 study designed to evaluated analgesic efficacy and safety of S-Ibuprofen Topical Gel 5%

Clinical Trial Description

The purpose of this randomized, double-blind study is to evaluate the efficacy and safety of S-Ibuprofen Topical Gel 5% in reducing pain/soreness associated with delayed onset muscle soreness (DOMS). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03852459
Study type Interventional
Source Aponia Laboratories, Inc.
Contact
Status Completed
Phase Phase 2
Start date January 12, 2018
Completion date April 11, 2019
View Details
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