Outcome Analysis in Septorhinoplasty

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorFRANK DECLAU

About this trial

A prospective observational cohort study that measures pre- and postoperative outcome of septorhinoplasty by means of patient-related outcome measures (PROMS: NOSE, FACE-Q, Utrecht Questionnaire, SCHNOS and BDDQ-AS) as well as with functional tests (NAR, AR, PNIF).

Eligibility criteria

Qualifiers

at least 18 years old

Patients eligible for external septorhinoplasty: patients seen in consultation because of nasal obstruction were evaluated. Patients who had symptoms of nasal obstruction for at least 1 year that were the result of an identifiable anatomical cause such as septal deviation, turbinate hypertrophy, internal valve collapse, or external valve collapse were included in the study.

Disqualifiers

< 18 years

mental or physical incapacity to answer the questionnaires

nasal fracture or surgery in the past year

nasal cocaine use in the past year

Trial design

Treatments tested in this trial

  • External septorhinoplasty

Treatment groups

No treatment groups listed

Sponsors and collaborators

FRANK DECLAU

Lead sponsor

Universiteit Antwerpen

Sponsor institution

Universiteit Antwerpen

Collaborator

Gasthuis Zusters Antwerpen

Collaborator