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).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
42
One Loxoprofen Pain Patch (active NSAID) applied once daily for 3 days
One Placebo Patch applied daily for 3 days
No Treatment for 3 days
Jean Brown Research
Salt Lake City, Utah, United States
Sum of pain intensity differences over 24 hours from baseline (SPID 24) with movement
Time frame: 0-24 hours
Sum of pain intensity differences over 24 hours from baseline (SPID 24) at rest
Time frame: 0-24 hours
Sum of pain intensity differences over 48 hours from baseline (SPID 48) with movement
Time frame: 0-48 hours
Sum of pain intensity differences over 48 hours from baseline (SPID 48) at rest
Time frame: 0-48 hours
Time to onset of first perceptible pain relief
Time frame: First 4 hours after Dose 1
Time to onset of meaningful pain relief
Time frame: First 4 hours after Dose 1
Subjects global impression of medication
Time frame: Day 10
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