Clinical experience with silver oxide-containing hydroxyapatite coated spinal interbody implant : prospective multicenter study
Not Applicable
Recruiting
- Conditions
- lumbar degenerative disease
- Registration Number
- JPRN-UMIN000039964
- Lead Sponsor
- Department of orhtopedics surgery, Saga university
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 250
Inclusion Criteria
Not provided
Exclusion Criteria
prior lumbar surgery
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method bone fusion rate(6month, 1 ,2 year)
- Secondary Outcome Measures
Name Time Method adverse events(infection rate, implant loosening, argria)