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Pediatric Hepatic Tumors (HEPATOBIO)

G

Gustave Roussy

Status

Enrolling

Conditions

Liver Tumor

Study type

Observational

Funder types

Other

Identifiers

NCT04274868
2015-A00180-49

Details and patient eligibility

About

Centralized biological collection of multicentric origin, retrospective and prospective of biological samples (tissues and fluids) taken within the framework of the diagnostic and therapeutic management of children and adolescents with liver tumor, and supported in the centers of French Society for Childhood Cancers (SFCE) with associated clinical database.

Enrollment

600 estimated patients

Sex

All

Ages

Under 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

    • 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.
    • 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.
    • 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

Trial design

600 participants in 1 patient group

Children and adolescents with liver tumor
Description:
Patients treated after 01/01/1990 for a primary liver tumor before the age of 18.

Trial contacts and locations

1

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Central trial contact

Brenda Mallon

Data sourced from clinicaltrials.gov

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