A prospective randomised clinical trial to assess change in nasal soft tissue dimensions in orthognathic surgery evaluated using a 3D imaging system
Completed
- Conditions
- Surgery: Dentofacial anomalies [including malocclusion]SurgeryDentofacial anomalies [including malocclusion]
- Registration Number
- ISRCTN38986023
- Lead Sponsor
- Record Provided by the NHSTCT Register - 2007 Update - Department of Health
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 64
Inclusion Criteria
1. Patients requiring a Le Fort 1 osteotomy to correct malocclusion
2. Patients concurrently undergoing a course of orthodontic fixed appliance therapy at the time of surgery
Exclusion Criteria
1. Patients have no previous history of facial trauma
2. Patients do not have a cleft lip and/or palate
3. Patients do not have a craniofacial abnormality
4. Patients are not undergoing a re-treatment procedure
5. Patients have not had previous facial soft tissue surgery
6. No children <16 years old
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method