Portable Navigation vs Conventional Instrument for Total Hip Arthroplasty:Prospective Randomized Trial
Not Applicable
- Conditions
- Hip Osteoarthritis, Osteonecrosis of femoral head, Rapidly destructive coxarthropathy, Rhumatoid arthritis, Proximal femoral fracture
- Registration Number
- JPRN-UMIN000030335
- Lead Sponsor
- Asahikawa Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 110
Inclusion Criteria
Not provided
Exclusion Criteria
Neuromuscular disease, Osteomalasia, Severe osteoporosis, Bone metabolic disease, Infection around hip, Severe bone loss, Other conditions judged to be inadequate for participation in the trial
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method