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 @ 4:55 AM
Ignite Modification Date:
2025-12-25 @ 4:55 AM
NCT ID:
NCT01947218
Eligibility Criteria:
Inclusion Criteria:
* The patient must be given free and informed consent and signed the consent
* The patient must be a member or beneficiary of a health insurance plan
* Women and men are included (s)
* The patient is aged at least 18 years
Exclusion Criteria:
* neoplastic disease extent
* Other progressive lung disease (tuberculosis, diseases of the pulmonary interstitium, active or recent pulmonary infection.)
* Patient unstable or had experienced exacerbation in the previous month study.
* Unable to understand the nature and purpose of the study
* Not affiliated to the French social security
* Making their military or military service career
* During periods of exclusion on another protocol
* Patients who are mentally or legally can not give consent.
* Patients with recent psychiatric disorders (less than a year).
* The illicit drugs or alcohol.
* Pregnant women, nursing mothers and women in labor;
* Women of childbearing potential without effective contraception (specified in the protocol)
* Persons deprived of their liberty by a judicial or administrative decision, hospitalized without consent and persons admitted to a health or social establishment for purposes other than research;
* Minors;
* The adults subject to a measure of legal protection or unable to consent;
* The people in emergency situations can not give consent.
* People with a cons-indication for bronchial biopsies (coagulation disorders, anticoagulation can be suspended ...)
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
80 Years
Study:
NCT01947218
Study Brief:
Protocol Section:
NCT01947218