Evaluation of the effect of polyethylene prosthesis on volume changes in mid-facial area
Not Applicable
Recruiting
- Conditions
- Midface Deficiency.Congenital malformation of face and neck, unspecified
- Registration Number
- IRCT20180515039664N1
- Lead Sponsor
- Islamic Azad University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 15
Inclusion Criteria
Patients requiring surgical prosthetics referring to Boouli Hospital
No systemic disease limiting ASA1 or ASA2 classifications
No history of surgery or trauma in the head and neck area
Exclusion Criteria
Infection or displacement of the prosthesis after surgery
BMI changes over one unit in the follow-up period
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Volume of the midfacial area. Timepoint: Measuring the volume of the face will be done before surgery and 5 months after surgery. Method of measurement: 3D scanner device Structured Light (Sense™, 3D Systems Inc, Rock Hill, USA).
- Secondary Outcome Measures
Name Time Method