The survey study of Dual-Mobility-THA for femoral neck fracture, on the indication and the efficacy/safety
- Conditions
- Femoral neck fracture
- Registration Number
- JPRN-UMIN000010625
- Lead Sponsor
- Stryker Japan K.K.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 50
Not provided
1) Patients have bacterial infectious disease or have risk highly of bacterial infection. 2) Patients have treatment history of acetabulum/ femur. 3) Patients, who are morbidly obese, defined as having a Body Mass Index (BMI) > 40. 4) Patients who is pregnant female or maybe so. 5) Patients who have a neuromuscular or neurosensory deficiency, which limits ability to evaluate the safety and efficacy of the device. 6) Patients with diagnosed systemic disease (i.e. Paget's disease, renal osteodystrophy), which limits ability to evaluate the safety and efficacy of the device. 7) Patients who are immunologically suppressed or receiving chronic steroids, which limits ability to evaluate the safety and efficacy of the device. 8) Patients who are judged ineligible with reasonable reason by primary doctor.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Functional evaluation QOL evaluation
- Secondary Outcome Measures
Name Time Method