Eligibility Module

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 @ 9:18 PM
Ignite Modification Date: 2025-12-24 @ 9:18 PM
NCT ID: NCT04451304
Eligibility Criteria: Inclusion Criteria: * All patients diagnosed with retinoblastoma and submitted to intra-arterial chemotherapy during the study period * Informed consent form signed and dated by legal guardian and investigator * Informed assent form signed by the patient if appropriate Exclusion Criteria: * Refusal of the patient or guardian to participate in the research project
Healthy Volunteers: False
Sex: ALL
Maximum Age: 18 Years
Study: NCT04451304
Study Brief:
Protocol Section: NCT04451304