Clinical trial of porous bioactive titanium for lumbar spine fusio
Not Applicable
- Conditions
- umbar disc disease, lumbar spondylolisthesis, lumbar isthmic spondylolisthesis
- Registration Number
- JPRN-UMIN000001448
- Lead Sponsor
- Kyoto University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 5
Inclusion Criteria
Not provided
Exclusion Criteria
1) No hip and leg disease 2) No cervical or thoracic spine disease 3) No previous lumbar spinal fusion 4) No collagen disease 5) BMI over 30 6) No pregnancy 7) No severe osteoporosis 8) No uncontrolable general disease 9) No malignacy 10) No psychological disease 11) No severe bacterial disease 12) No steroid treatment
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intraoperative handling of the implant and avoidance of iliac crest bone graft harvesting.
- Secondary Outcome Measures
Name Time Method