Using Continuous Passive Motion for Patients with Pelvic and Knee Fractures
Official title: The Role of Continuous Passive Motion in Pain Control of Patients Undergoing Operative Management of Isolated Acetabular Fractures, Supracondylar Femur Fractures, or Tibial Plateau Fracture: A Comparative Study
Run by University of Cincinnati · NCT04389749 · Data updated 2026-11-12
This study is testing if a special movement therapy after surgery for pelvic and knee fractures can help patients feel less pain and recover better compared to regular care.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 100 (estimated) |
| Sponsor | University of Cincinnati Academic / other |
| Locations | 1 site (Cincinnati, Ohio) |
| Status | Recruiting |
| Started | October 6, 2020 |
| Main results expected | June 2026 |
| Study ends | June 2027 |
| Registry record updated | May 4, 2026 |
| Trial ID | NCT04389749 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults over 18 who have had open reduction and internal fixation for isolated acetabular, supracondylar femur, or tibial plateau fractures.
✕Probably not a fit
Patients with injuries affecting their ability to bear weight or those under 18, pregnant, or incarcerated may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study compares the effectiveness of continuous passive motion (CPM) therapy against standard care in patients who have undergone surgery for specific types of fractures. Participants will be randomized into two groups: one receiving CPM therapy immediately post-surgery and the other receiving typical postoperative care. The study will assess pain levels and narcotic medication use during the hospital stay, as well as functional outcomes one year after surgery. Data will be collected on visual analog scale scores and monitored for any adverse events.
Why it matters
Potential benefit: If successful, this approach could lead to reduced pain and lower narcotic use for patients recovering from pelvic and knee fractures.
How similar studies have gone: Previous studies have shown promising results with CPM in similar orthopedic contexts, suggesting potential benefits in pain management and recovery.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age 18 or greater * Isolated acetabular fractures, supracondylar femur fractures, or tibial plateau fracture * Have undergone operative intervention for fracture Exclusion Criteria: * Injury to either lower extremity that affects the patient's ability to weight bear * Under the age of 18 * Pregnant * A prisoner
Where it's running
-
Univrsity of Cincinnati Medical Center
Cincinnati, Ohio, United States Recruiting
Study contacts
- Principal investigator: Henry C Sagi, MD — University of Cincinnati
- Study coordinator: Kimberly A Hasselfeld, MS
- Email: hasselky@uc.edu
- Phone: 513-558-1933
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.