Evaluation of Distraction osteogenesis for severe hypoplastic maxilla or mandible
Not Applicable
- Conditions
- Hypoplastic maxilla, hypoplastic mandible
- Registration Number
- JPRN-UMIN000004402
- Lead Sponsor
- Tohoku University Graduate School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Not provided
Exclusion Criteria
drop out until 1 year postoperative
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method evaluation at a month, 6months, 12months after the operation complication occlusion collapse of distracted segments velopharyngeal function
- Secondary Outcome Measures
Name Time Method
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 pathways are involved in distraction osteogenesis for hypoplastic maxilla/mandible?
How does distraction osteogenesis compare to orthognathic surgery in treating severe hypoplastic maxilla or mandible?
Which biomarkers predict successful bone regeneration in distraction osteogenesis for craniofacial hypoplasia?
What are the common adverse events associated with distraction osteogenesis in severe hypoplastic jaw conditions and their management?
Are there combination therapies with growth factors enhancing distraction osteogenesis outcomes in hypoplastic mandible/maxilla?