Comparing early weight bearing with weight bearing restriction after hip fracture surgery
Compare Early Weight Bearing as Tolerated (WBAT) Group With Weight Bearing Restriction(WBR) After Hip Fracture Nailing,
This study tests whether allowing older patients to put weight on their hip sooner after surgery for a hip fracture helps them recover better than if they have to wait.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 65 Years and up |
| Sex | All |
| Sponsor | Far Eastern Memorial Hospital Academic / other |
| Locations | 1 site (New Taipei City) |
| Trial ID | NCT06329271 on ClinicalTrials.gov |
What this trial studies
This clinical trial investigates the effects of early weight bearing as tolerated (WBAT) versus weight bearing restriction (WBR) in elderly patients who have undergone proximal femur fracture fixation. A total of 60 geriatric patients with AO/OTA type 31 fractures will be recruited and randomly assigned to either the WBAT or WBR group. The study will assess clinical outcomes such as functional hip scores, pain levels, and complications, while also monitoring radiological parameters and ambulation status over time.
Who should consider this trial
Good fit: Ideal candidates are elderly patients with AO/OTA type 31 proximal femur fractures who are undergoing intramedullary nail fixation.
Not a fit: Patients with pathological fractures, significant comorbidities, or those at high risk of falling may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved recovery times and functional outcomes for elderly patients after hip fractures.
How similar studies have performed: Previous studies have shown promising results with early weight-bearing protocols in similar populations, suggesting potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients with AO/OTA type 31 fractures were included, and all fractures were classified using intraoperative fluoroscopy with traction on the fracture table. Exclusion Criteria: * Patients with pathological fractures, neurovascular insufficiency, ipsilateral lower extremity musculoskeletal injury, multiple fractures, or high risk of falling, including frequent falling accidents within 6 months, unsteady gait, ipsilateral neuropathy, limb weakness, and urinary incontinence were excluded.
Where this trial is running
New Taipei City
- Far-Eastern Memorial Hospital — New Taipei City, Taiwan (Recruiting)
Study contacts
- Study coordinator: Yen Cheng Chen, Doctor
- Email: sstteevveepp@gmail.com
- Phone: 886-919207805
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.