Expired Study
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Salt Lake City, Utah 84124


Purpose:

The purpose of this study is to evaluate the analgesic efficacy and safety of a new pain patch compared to placebo and no treatment in subjects experiencing Delayed Onset Muscle Soreness (DOMS).


Criteria:

Inclusion Criteria: - Males or females, 18 to 40 years of age - are in good general health, with a BMI less than or equal to 32, and able to perform the exercise regimen - develops muscle pain/soreness within 24-48 hours of the end of the exercise regimen and have a baseline muscle pain/soreness with movement of greater than or equal to 5 on the Numerical Rating Scale (NRS) (numerical rating scale) and at least "moderate" on the categorical scale Exclusion Criteria: - has engaged in upper extremity exercise for a minimum of 6 months prior to study participation - has been working heavy manual or physical labor jobs within 3 months prior to study participation. - has a known history of allergic reaction or clinically significant intolerance to acetaminophen, aspirin, or any nonsteroidal anti-inflammatory drugs - has skin lesions such as psoriasis at the application site - has abnormal skin condition such as eczema, contact dermatitis, pigment anomaly, etc. - has an allergy-related skin condition


NCT ID:

NCT02602353


Primary Contact:

Principal Investigator
Derek Muse, MD
Jean Brown Research


Backup Contact:

N/A


Location Contact:

Salt Lake City, Utah 84124
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 21, 2020

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