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 @ 3:33 PM
Ignite Modification Date: 2025-12-24 @ 3:33 PM
NCT ID: NCT02607592
Eligibility Criteria: Inclusion Criteria: 1. Patient who was confirmed primary adenocarcinoma by pathologic histology or cytology 2. The TNM staging system according to IASLC2009 was stageIV or those stageIIIB who were not fit for operation or radiotherapy 3. Including one available evaluation lesion at least according to RECIST criteria 4. Adult patients (≥18 years and ≤75 years). ECOG Performance Status 0 or 1 .Life expectancy of at least 12 weeks.Haemoglobin ≥90g/dl, Absolute neutrophil count (ANC)≥ 2x 109/L, platelets ≥100 x 109/L. Total bilirubin ≤upper limit of normal (ULN). ALT and AST ≤ 2.5 x ULN. Creatinine clearance ≥60ml/min (calculated according to Cockcroft-gault formula). 5. Patients who had never received any antineoplastic therapy Exclusion Criteria: 1. Patient who has another cancer in recent 5 years,not including basal cell carcinoma or cervical carcinoma in situ 2. Patient with brain metastases whose intracranial pressure symptoms can not control by using glucocorticoid or mannitol 3. Previous radiotherapy(Palliative radiotherapy in order to pain management can be excluded) 4. Patient who has used chemotherapy before(bisphosphonate can be excluded ) 5. Serious uncontrolled systemic disease including active infection,uncontrolled hypertension,diabetes,unstable angina,congestive heart failure,myocardial infarction,severe arrhythmia which needs drugs,hepatic、renal and metabolic disease 6. Patient who is allergic to drugs we need to use 7. Patients who are in pregnancy or lactation 8. AST or ALT 》2.5 \* upper limit of normal (ULN),and ALP》5\*ULN
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Maximum Age: 75 Years
Study: NCT02607592
Study Brief:
Protocol Section: NCT02607592