Study to Evaluate the Efficacy of the Synera Patch Compared to Naproxen Sodium for Epicondylitis of the Elbow

Epicondylitis of the Elbow Clinical Trial

Official title:
Randomized, Parallel-Group, Open Label, Dose Finding Study to Evaluate the Efficacy of Synera Patch Compared to Naproxen Sodium for the Treatment of Lateral and Medial Epicondylitis of the Elbow

Status Completed

Clinical Trial Summary

The purpose of the this study is to evaluate the sfaety and efficacy of Synera(R)for patients with lateral and medial epicondylitis and compare it to Naproxen sodius.

Clinical Trial Description

The objective of this single center is to evaluate the safety and efficacy of Synera ® in lateral and medial epicondylitis . This is an open-label, comaparative study study where the subjects will be randomized to one of the following groups:

1. Synera patch ®: A single patch applied for 4 hours twice daily approximatey 12 hrs apart to the medial or lateral side of the index elbow

2. Synera patch ®: A single patch applied for 12 hours/day to the medial or lateral side of the index elbow

3. Naproxen Sodium: 500mg bid ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01525043
Study type	Interventional
Source	International Clinical Research Institute
Contact
Status	Completed
Phase	Phase 4
Start date	February 2012
Completion date	September 2013

View Details

See also
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Completed	`NCT04856228` - Radial Tunnel Syndrome in Resistant Lateral Epicondylitis	N/A