RecruitingNCT07257094

Nasal Reconstruction FACE-Q : French Validation of the Nasal Reconstruction FACE-Q Questionnaire for Reconstruction/Rehabilitation Following Nasal Skin Cancer

French Validation of the Nasal Reconstruction FACE-Q Questionnaire for Reconstruction/Rehabilitation Following Nasal Skin Cancer


Sponsor

Hôpital NOVO

Enrollment

346 participants

Start Date

Jan 10, 2026

Study Type

OBSERVATIONAL

Conditions

Summary

This study aims to validate a French version of the Nasal Reconstruction FACE-Q questionnaire for patients who have undergone nasal reconstruction or prosthetic rehabilitation after surgery for nasal skin cancer. The questionnaire evaluates appearance, quality of life, and possible side effects related to the reconstruction. The investigators hypothesize that the validated French version will provide a reliable and standardized tool to assess patient satisfaction and health-related quality of life in this context.


Eligibility

Min Age: 18 Years

Inclusion Criteria13

  • PATIENTS
  • Age ≥ 18 years
  • Patient who has undergone excision of a cutaneous, mucocutaneous, or vestibular nasal cancer with surgical reconstruction using a flap or prosthetic rehabilitation, performed more than 4 months ago, with stable results, and less than 3 years ago
  • Patient informed of the study and not opposed to participation
  • Age ≥ 65 years
  • Subject informed and not opposed to participating in the study
  • Subject who has never undergone facial trauma or surgery, and without major comorbidity, defined as follows:
  • No heart failure (moderate or severe heart failure, history of heart attack within the last 6 months);
  • No severe chronic respiratory disease (no stage III-IV COPD, no prolonged oxygen therapy);
  • No uncontrolled diabetes or associated severe complications;
  • No active immunosuppressive diseases or high-dose immunosuppressive treatment;
  • No unstable or severe facial dermatological conditions;
  • No comorbidities seriously affecting quality of life or respiratory function (at the investigator's discretion).

Exclusion Criteria9

  • Patient under anticoagulant or antiplatelet therapy Non-French-speaking patient
  • Patient under legal protection (e.g., guardianship, legal safeguard) or with limited legal capacity
  • Patient unlikely to cooperate with the study and/or poor anticipated compliance as judged by the investigator (including psychiatric disorders other than depressive disorder or cognitive impairment)
  • Pregnant or breastfeeding woman
  • CONTROL
  • Non-English speaking subject
  • Subject under guardianship or legal protection, legally incompetent or with limited legal capacity
  • Subject unlikely to cooperate in the study and/or anticipated low cooperation by the investigator (particularly those with psychiatric disorders other than depression or cognitive disorders)
  • Pregnant or breastfeeding women

Interventions

OTHERoperated patients

Response to the Nasal Reconstruction FACE-Q questionnaire, which includes the following scales : * Appearence : Face overall, nose, nostrils, skin * Health related quality of life (HRQOL) : Early life impact, psychological, social, outcome * Adverse effects : on the nose, on the forehead, eyebrows and scalp * Nasal Obstruction Symptom Evaluation (NOSE) * Short-Form-36 (SF 36)

OTHERControl

Response to the Nasal Reconstruction FACE-Q questionnaire, which includes the following scales : * Appearence : Face overall, nose, nostrils, skin impact psychological, impact social, * SF36


Locations(9)

CHU Caen

Caen, France

Centre Antoine Lacassagne

Nice, France

Institut Curie

Paris, France

Hôpital Lariboisière (AP-HP)

Paris, France

Hôpital Bichat (APHP)

Paris, France

Hopital Novo

Pontoise, France

HNIA Toulon

Toulon, France

CHU Toulouse

Toulouse, France

Institut Gustave Roussy

Villejuif, France

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07257094


Related Trials