Clinical trial on the effect of difference in surgical procedure for treating adult spinal deformity
Not Applicable
- Conditions
- Adult spinal deformity
- Registration Number
- JPRN-UMIN000033082
- 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
- 90
Inclusion Criteria
Not provided
Exclusion Criteria
1. Subjects who have had spinal fixation. 2. Subjects who are pregnant or will be possibly pregnant. 3. Subjects who have an allergy to nickel, chromium, or Titanium alloy. 4. Subjects who have an actively spinal infection. 5. Subjects who are an inappropriate for participating in the study in the judgement of the investigator.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Radiographic outcomes and QOL improvement rate at the 24 months follow-up
- Secondary Outcome Measures
Name Time Method