Multi-centric randomized open-label comparative study for influence of bisphosphonate on fracture healing in patients with spinal compression fractures or femoral neck fractures
Not Applicable
- Conditions
- Osteoporotic spinal compression fractures and femoral neck fractures
- Registration Number
- JPRN-UMIN000000838
- Lead Sponsor
- Department of Orthopaedic Surgery, Dokkyo Medical University Koshigaya Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
Exclusion criteria are patients treated with bisphosphonate within 3 months, fractures resulted from high energy trauma, patients contraindicant to bisphosphonate, and patients judged inadequate to include this study by doctors.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Fracture healing is assessed with X ray film and computed tomograhy, and QOL is assessed with questionnaires.
- Secondary Outcome Measures
Name Time Method Bone mineral density, visual analogue scale and bone markers are measured.