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:
2025-12-24 @ 5:38 PM
Ignite Modification Date:
2025-12-24 @ 5:38 PM
NCT ID:
NCT04274868
Eligibility Criteria:
Inclusion Criteria:
1. \- For inclusion in the clinical database:
* Children and adolescents (≤18 years at diagnosis) suffering from a primary liver tumor diagnosed after 01/01/1990 and treated in France
* Informed consent to the computerization of data signed by the patient or by parents or legal representatives if he is a minor.
2. \- For inclusion in the biological collection (CRB Paris Sud):
* Additional criteria:
* Availability of biological samples (tumor tissue, healthy tissue, plasma and / or serum).
* Informed consent to the use of biological remains signed by the patient or by parents or legal representatives if he is a minor.
3. \- For the inclusion of deceased patients:
* Obtaining consent or failing this, seeking non-opposition to the computerization of data (for inclusion in the database) and the use of biological remains (for inclusion in the biological collection) of the patient or both parents or the legal guardian if he is a minor.
Exclusion Criteria:
* None
Sex:
ALL
Maximum Age:
18 Years
Study:
NCT04274868
Study Brief:
Protocol Section:
NCT04274868