Actively Recruiting

Age: 18Years +
All Genders
ID03925389

Functional and Aesthetic Outcome Analysis in External Septorhinoplasty

Led by FRANK DECLAU · Updated on 2025-03-27

750

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

F

FRANK DECLAU

Lead Sponsor

U

Universiteit Antwerpen

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating the functional and aesthetic outcomes in patients undergoing external septorhinoplasty, a surgical procedure to correct nasal structure for both appearance and breathing improvement. This prospective observational cohort study measures patient satisfaction and nasal function before and after surgery using various questionnaires and functional tests. The study aims to capture changes over time to better understand patient outcomes following septorhinoplasty. Participants will undergo external septorhinoplasty, a surgery involving an external incision at the columella to repair defects of the nasal septum and external nasal pyramid. Patient-related outcome measures including NOSE, FACE-Q, Utrecht Questionnaire, SCHNOS, and BDDQ-AS are collected preoperatively and at 3, 6, and 12 months postoperatively. Functional tests such as nasal anterior rhinomanometry, peak nasal inspiratory flow, and acoustic rhinometry are performed before surgery and then again at 6 and 12 months after surgery. During the study, participants will complete detailed questionnaires about nasal obstruction and aesthetic satisfaction at several time points. Functional nasal tests will be conducted to objectively assess nasal airflow and structure. Researchers will analyze the changes in these measurements over one year to evaluate the impact of surgery. Patient demographics and nasal history will also be collected to correlate with outcomes. The total participation duration includes assessments up to 12 months after surgery to monitor long-term effects.

CONDITIONS

Brief Title

Outcome Analysis in Septorhinoplasty

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • At least 18 years old
  • Patients eligible for external septorhinoplasty
  • Symptoms of nasal obstruction for at least 1 year caused by identifiable anatomical issues such as septal deviation, turbinate hypertrophy, internal valve collapse, or external valve collapse
Not Eligible

You will not qualify if you...

  • Younger than 18 years
  • Mental or physical incapacity to answer questionnaires
  • Nasal fracture or surgery in the past year
  • Nasal cocaine use in the past year

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 screening and enrollment visit (in-person)

Surgery and Immediate Post-operative Care

Duration - Day of surgery plus immediate recovery period

Participants undergo an external septorhinoplasty, a surgical procedure to repair defects or deformities of the nasal septum and external nasal pyramid.

1 surgical visit (in-person)

Post-operative Follow-up

Duration - 12 months

Participants are followed up to assess functional and aesthetic outcomes using questionnaires and functional nasal tests.

Visits at 3, 6, and 12 months postoperatively (in-person)

Trial Site Locations

Total: 1 location

1

Dept. Otorhinolaryngology, H&N Surgery

Antwerp, Belgium, 2018

Actively Recruiting

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Research Team

F

Frank Declau, MD, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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Published Research Related To This Trial

Piezo-assisted Turbinoplasty Versus Partial Turbinectomy in External Septorhinoplasty: A Prospective Comparative Study in 100 Patients.

Valérie Verkest, Laura Pingnet, Erik Fransen...

https://pubmed.ncbi.nlm.nih.gov/35022839