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A Study Comparing the Efficacy and Safety of Orally Administered Ibuprofen and Placebo in Delayed Onset Muscle Soreness — DOMS  

Delayed Onset Muscle Soreness Clinical Trial

Official title:
A Double-Blind, Repeat-Dose, Parallel Group Study Comparing the Efficacy and Safety of Orally Administered Ibuprofen and Placebo in Delayed Onset Muscle Soreness.

Clinical Trial Summary

The hypotheses to be tested are: Efficacy: Ibuprofen will be more effective than the Placebo in relieving muscle pain/soreness over 48 hour post-dosing with study medication. Safety: There will be no or minimal increased incidence of adverse events (AEs) with Ibuprofen versus and both will be well tolerated.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02113566
Study type Interventional
Source Jean Brown Research
Contact
Status Completed
Phase Phase 4
Start date February 2013
Completion date May 2013
View Details
See also
  Status Clinical Trial Phase
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Completed NCT02157675 - Effects of a Polyherbal Supplement on the Signs and Symptoms of Delayed Onset Muscle Soreness Phase 4