Efficacy of custom made tool for reducing facial swelling after maxillofacial surgery
Not Applicable
- Conditions
- facial fracture.Fracture of skull and facial bones
- Registration Number
- IRCT2016040427214N1
- Lead Sponsor
- Kerman University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 14
Inclusion Criteria
Patients who have similar bilateral fractures of the upper or lower of jaw; Patients who need surgery for incising soft tissue similar in both sides; Patients who need orthognathic surgery for similar osteotomy upper or lower jaw
Exclusion criteria: Patients who have asymmetry in their examination; Patient who has a previous history of oral and maxillofacial surgery; Patient who has severe damage and unusual soft tissue swelling after trauma; Patients with systemic diseases such as diabetes mellitus affecting the healing process and swelling; Patients who do not have cooperation during the study
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Swelling. Timepoint: Pre operation time,After surgery,1,2 and 7 days after surgery. Method of measurement: Millimeter.
- Secondary Outcome Measures
Name Time Method