A Within-subject Study to Evaluate the Efficacy and Safety of Diclofenac Sodium Topical Gel 1% Compared to Placebo in Subjects Experiencing Delayed Onset Muscle Soreness

PHASE3CompletedINTERVENTIONAL
Enrollment

102

Participants

Timeline

Start Date

October 31, 2014

Primary Completion Date

December 31, 2014

Study Completion Date

December 31, 2014

Conditions
Muscle Soreness
Interventions
DRUG

Diclofenac sodium gel 1%

Diclofenac sodium gel 1% four times daily (This study is a within-subject design i.e. active drug applied to one leg and placebo to the other leg at the same time. Therefore the study design is not a cross-over).

DRUG

Placebo

Placebo gel four times daily (This study is a within-subject design i.e. active drug applied to one leg and placebo to the other leg at the same time. Therefore the study design is not a cross-over).

Trial Locations (1)

91105

Lotus Clinical Research, 100 W California Blvd,, Pasadena

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Novartis

INDUSTRY