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 @ 1:39 PM
Ignite Modification Date:
2025-12-24 @ 1:39 PM
NCT ID:
NCT05811195
Eligibility Criteria:
Inclusion Criteria:
* Diagnosis of malignant neoplasia (hematological or solid tumors);
* Responsible and participants agree to the study participation after reading and signing the Informed Consent Form (ICF) and Informed Term of Consent (TALE) for participation in Clinical Research;
* They performed the chemotherapy infusions hospitalized in the pediatric oncology department of the 3rd east of HCPA;
* Received the following chemotherapy protocols: MTX-HD, combination chemotherapy of MTX-HD, doxorubicin and cyclophosphamide; and MTX-HD and cyclophosphamide.
Exclusion Criteria:
* Participants will be excluded who:
* Patients over the age of 18 years
* Patients who will undergo HSCT
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
1 Month
Maximum Age:
18 Years
Study:
NCT05811195
Study Brief:
Protocol Section:
NCT05811195