About this trial
CERNAS is a prospective, multicenter, non-interventional study comparing the functional and aesthetic outcomes of two rehabilitation strategies after total or subtotal nasal amputation: surgical reconstruction (primarily paramedian forehead flap or free flap) versus nasal epithesis (prosthesis). Patients who have undergone either rehabilitation at least one year prior to enrolment will be invited to complete the validated French version of the SCHNOS (Standardized Cosmesis and Health Nasal Outcomes Survey) questionnaire. The study aims to provide an objective, patient-reported comparison of these two options to guide future clinical decision-making.
Eligibility criteria
Qualifiers
Patients aged 18 years or older
Patients who have undergone total or subtotal nasal amputation (defined as loss of at least three nasal subunits, or of two subunits including the dorsum) and who have been rehabilitated either by surgical reconstruction or by nasal epithesis for more than one year
Disqualifiers
Ongoing tumour progression or tumour recurrence
Non-French-speaking patients
Patients under legal protection measures (guardianship, legal safeguarding, limited or full legal incapacity)
Patients unlikely to cooperate with the study (e.g. presenting with a psychiatric disorder)
Trial design
Treatments tested in this trial
- SCHNOS score