Trials / Enrolling By Invitation
Enrolling By InvitationNCT07393503
Musculoskeletal Outcomes Using Tylenol/Ibuprofen vs. Oral Steroids in New Injuries
- Status
- Enrolling By Invitation
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- Sponsor
- State University of New York at Buffalo · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
In this pilot study, the investigators aim to compare two short-term pain relief methods administered over the course of 6 days in the setting of acute musculoskeletal (MSK) pain: 1. Methylprednisolone((Medrol)dose pack- standard taper per dose pack instructions 2. Standard of Care (SOC) which includes a combination of Acetaminophen (Tylenol)+Ibuprofen (Motrin) The investigators are interested in studying pain relief regimens for acute injury of any body part among an adult orthopaedic urgent care population.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Methylprednisolone 4Mg Tab | Participants follow standard 6- day taper dosing schedule. |
| DRUG | Acetaminophen 500Mg Tab | Participants follow a 6- day taper dosing schedule. |
| DRUG | Ibuprofen 200Mg Oral Tablet | Participants follow a 6- day taper dosing schedule. |
Timeline
- Start date
- 2025-09-17
- Primary completion
- 2026-08-01
- Completion
- 2027-01-01
- First posted
- 2026-02-06
- Last updated
- 2026-02-18
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT07393503. Inclusion in this directory is not an endorsement.