Development of custom-made surgical guide for osteotomy and screw insertion.
Phase 1
Recruiting
- Conditions
- Orthopedic patients to be undergone surgery with osteotomy or screw insertion.
- Registration Number
- JPRN-UMIN000004618
- Lead Sponsor
- Kyoto University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Not provided
Exclusion Criteria
1) Patient without computed tomography image with adequate resolution for the guide preparation. 2) Patient without enough time for the guide preparation. 3) Patient who considered as inadequate for participate this trial by the medical attendant responsible for this trial.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To avoid major vascular and neurological injury in association with osteotomy and screw insertion.
- Secondary Outcome Measures
Name Time Method Intra- and postoperative evaluation of efficacy and problem of the surgical guide.
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie the efficacy of custom-made surgical guides in osteotomy and screw insertion for orthopedic patients?
How does the use of custom-made surgical guides compare to standard-of-care techniques in terms of clinical outcomes for osteotomy procedures?
Are there specific biomarkers that can predict optimal patient selection for custom-made surgical guides in orthopedic surgeries?
What are the potential adverse events associated with custom-made surgical guides in orthopedic interventions and how are they managed?
What are the current trends in the development of surgical guides for osteotomy, including related compounds or combination approaches in orthopedic surgery?