Patient Satisfaction After Patient-specific Jawline Augmentation
Trial Snapshot
- Phase
- Not Applicable
- Enrollment
- 26
- Locations
- 1
- Primary Endpoint
- Satisfaction/Quality of Life
Study Overview
Brief Summary
The survey studies patient satisfaction after titanium patient specific jawline augmentation in congenital, post-trauma, deformity and transgender/cosmetic jaw angle/border deficiencies.
Detailed Description
Additively manufactured titanium implants have been pre-designed in the hospital department, further designed and manufactured by 2 Belgian companies. The issue is if all patients have satisfactory perception of the improvement of their morphology and the actual outcome of the procedure, and how theur social ineractions are perceived today.
Study Design
- Study Type
- Observational
- Observational Model
- Case Only
- Time Perspective
- Retrospective
Eligibility Criteria
- Ages
- 18 Years to 75 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •All lower jaw augmentation implants
Exclusion Criteria
- Not provided
Outcomes
Primary Outcomes
Satisfaction/Quality of Life
Time Frame: 1 year
By means of 4 surveys (social, psychological, outcome and satisfaction) based on FACE-Q. The scales can be used independently of the other scales.Higher scores reflect a better outcome. If missing data is less than 50% of the scale's items, insert the mean of the completed items. Use the Conversion Table to convert the raw summed scale score into a score from 0 (worst) to 100 (best).
Secondary Outcomes
No secondary outcomes reported
Investigators
Veerle Van Mossevelde
Principal Investigator
Universitair Ziekenhuis Brussel