Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 1:40 AM
Ignite Modification Date:
2025-12-25 @ 1:40 AM
NCT ID:
NCT07257094
Eligibility Criteria:
Inclusion Criteria:
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
CONTROL 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).
Translated with DeepL.com (free version)
Exclusion Criteria:
PATIENTS
* 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
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT07257094
Study Brief:
Protocol Section:
NCT07257094