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NCT02113566 · ClinicalTrials.gov registry record · Phase 4
A Study Comparing the Efficacy and Safety of Orally Administered Ibuprofen and Placebo in Delayed Onset Muscle Soreness
A Phase 4 study of Delayed Onset Muscle Soreness, sponsored by Jean Brown Research.
- Completed
- Registry status
- Phase 4
- Development phase
- 60
- Enrollment target
- 1
- Study location
NCT02113566: Completed Phase 4 study of Delayed Onset Muscle Soreness, sponsored by Jean Brown Research.
NCT02113566 is a Phase 4 study of Delayed Onset Muscle Soreness that has completed, run by Jean Brown Research. The registered enrollment target is 60 participants, above the 31-participant average among 3 other Delayed Onset Muscle Soreness trials with a reported enrollment target (94% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02113566, a Phase 4 study of Delayed Onset Muscle Soreness, has completed, sponsored by Jean Brown Research.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 60 participants
- Enrollment target
- 1
- Study location
Study 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.
Primary Outcome
The primary efficacy parameter is muscle pain/soreness with movement at 48 hours (SPID 0-48)
Conditions Studied
Interventions
- DRUG Acetaminophen 1000mg
Study Locations (1)
Utah
- Jean Brown Research - Salt Lake City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2013-02 |
| Est. Completion | 2013-05 |
| Phase | Phase 4 |
What the finished NCT02113566 record still lists
NCT02113566 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, above the 31-participant average among 3 other Delayed Onset Muscle Soreness trials with a reported enrollment target (94% higher).
The record links to 1 condition, with Delayed Onset Muscle Soreness appearing as the primary indexed condition, and to 1 intervention - of which Acetaminophen 1000mg is the first listed.
NCT02113566 reports a single indexed study location in Utah.
Frequently Asked Questions
What is clinical trial NCT02113566 about?
NCT02113566 is a clinical study titled "A Study Comparing the Efficacy and Safety of Orally Administered Ibuprofen and Placebo in Delayed Onset Muscle Soreness". 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 t...
What is the current status of trial NCT02113566?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 60 participants. The study started on 2013-02. Estimated completion is 2013-05.
What conditions does trial NCT02113566 study?
This clinical trial studies the following conditions: Delayed Onset Muscle Soreness.
What interventions are being tested in trial NCT02113566?
The interventions under investigation include: Acetaminophen 1000mg (DRUG).
Who is sponsoring clinical trial NCT02113566?
This trial is sponsored by Jean Brown Research, which has 2 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02113566 being conducted?
This trial has 1 study location across Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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