CClinicalTrials.gg
Status unknownNCT03932734Updated Jul 30, 2019

Patient Satisfaction After Patient-specific Jawline Augmentation

An observational study in Congenital Deformity of Face and Post-traumatic Deformity, sponsored by Universitair Ziekenhuis Brussel. Status unknown at 1 site in Belgium. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2019-07-30.

Sponsored by Universitair Ziekenhuis Brussel · Observational

The sponsor has not verified this record recently (last verified Jul 2019), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Case-only
Time perspective
Retrospective
Enrollment
26
Ages
18 Years to 75 Years
Sex
All
01

Study summary

The survey studies patient satisfaction after titanium patient specific jawline augmentation in congenital, post-trauma, deformity and transgender/cosmetic jaw angle/border deficiencies.

Read the 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.

02

Conditions studied

  • Congenital Deformity of Face
  • Post-traumatic Deformity

Keywords

  • Satisfaction
  • Jawline augmentation
  • Transgender
  • Cosmetic jaw angle
03

In context

Congenital Abnormalities

980 studies on the registry are indexed under Congenital Abnormalities; 177 are open to participants now.

This study's planned enrollment of 26 is below the median of 153 across 446 observational studies indexed under Congenital Abnormalities.

Browse Congenital Abnormalities studies →

Lead sponsor

Universitair Ziekenhuis Brussel is the lead sponsor of 362 studies on the registry; 103 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All patients who had lower jaw augmentation implants since 2014 not gender based

Inclusion criteria

  • All lower jaw augmentation implants

Exclusion criteria

Exclusion Criteria:

  • N/A
05

Study design

Observational model
Case-only
Time perspective
Retrospective
Enrollment
26 participants (estimated)
Patient registry
No

Groups and cohorts

  • survey

    Other: survey

Interventions

  • Othersurvey

    Face-Q conversion table

06

What researchers measure

Primary outcomes

  1. Satisfaction/Quality of Life

    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).

    Time frame: 1 year

07

Study locations

1 of 1 sites recruiting
  • Universitair Ziekenhuis Brussel
    Jette, Vlaams Brabant 1090, Belgium
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 30, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT03932734
Lead sponsor
Universitair Ziekenhuis Brussel
Responsible party
Veerle Van Mossevelde (Principal Investigator, Universitair Ziekenhuis Brussel) — Principal investigator
First posted
May 1, 2019
Start date
Jun 30, 2019
Primary completion
Dec 1, 2019 (estimated)
Completion
Jan 31, 2020 (estimated)
Last update
Jul 30, 2019

Study contacts

Veerle Van Mossevelde, SC
Contact
veerle.vanmossevelde@uzbrussel.be
+3224763134
Maurice Mommaerts, Prof Mult
principal investigator · Universitair Ziekenhuis Brussel

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jul 2019. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion