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: 2025-12-26 @ 11:08 AM
Ignite Modification Date: 2025-12-26 @ 11:08 AM
NCT ID: NCT03913312
Eligibility Criteria: Inclusion Criteria: 1. AML patients diagnosed by bone marrow morphology and Immunology; 2. Exclusion of APL by Bone marrow morphology or molecular level; 3. A patient who has obtained bone marrow cytology remission after inductive treatment; 4. Aged from 60 to 75 years; 5. Liver and kidney function: blood bilirubin ≤ 35μmol / L, AST or/ALT \<2 times the upper limit of normal (ULN), serum creatinine;≤ 150μmol / L; 6. The function of Heart is normal; 7. Physical condition score 0-2 (ECOG score); 8. Get informed consent signed by patient or family member. Exclusion Criteria: 1. APL patients, treatment-related AML; 2. Retreatment of patients; 3. Allergies to any of the drugs involved in the protocol; 4. There are obvious contraindications to chemotherapy drugs; 5. Liver and kidney function is obviously abnormal, exceeding the inclusion criteria; 6. Serious heart disease, including myocardial infarction, cardiac insufficiency; 7. Suffering from other organ malignant tumors at the same time ; 8. Active period of tuberculosis patients and HIV-positive patients; 9. Suffering from other blood system diseases at the same time; 10. Pregnancy or breastfeeding; 11. Cannot understand or follow the research plan; 12. A history of intolerance or allergies to similar drugs; 13. Patients under 60 years of age or over 75 years of age; 14. Participate in other clinical researchers at the same time; 15. There are other situations that hinder the conduct of the study.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 60 Years
Maximum Age: 75 Years
Study: NCT03913312
Study Brief:
Protocol Section: NCT03913312