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: 2025-12-25 @ 2:02 AM
Ignite Modification Date: 2025-12-25 @ 2:02 AM
NCT ID: NCT02498860
Eligibility Criteria: Inclusion Criteria: * Adenocarcinoma of Lung * Postoperative pathologic stage IB\~IIIA * Complete surgical resection (R0 resection) N1-2: R0 resection with lobectomy and mediastinal lymph nodes dissection (MLND) N0: R0 resection with lobectomy with or without MLND * Adjuvant treatment should start between 4 to 6 weeks after surgery * ECOG performance status 0-1 * Weight loss during last 3 months should be less than 10%. * Normal hematologic, hepatic and renal function Neutrophil count \> 1500 /microliter, Platelet \> 100,000/microliter, Hemoglobin \> 9 g/dL Bilirubin \<=1.5 x upper limit normal, transaminase \< 2.5 x upper limit normal Serum Creatinine \<=1.5 mg/dL * Women in child bearing age should consent using contraceptive measures, and must have negative pregnancy test. Exclusion Criteria: * Other malignant neoplastic disease within 5 years. * Neoadjuvant chemotherapy before surgery of lung cancer * Patients who will be treated with postoperative radiation. * Stage IIIB or IV lung cancer * Severe infection, or cardiorespiratory, hematologic illness * HIV positive cases * Pregnancy or lactating women * Autoimmune diseases or those who receiving immune suppressive treatment * Symptomatic neuropathy \> CTCAE grade 1 * Those who consented other clinical trials within 3 months * Other significant medical conditions contraindicated to clinical trial
Healthy Volunteers: False
Sex: ALL
Minimum Age: 20 Years
Study: NCT02498860
Study Brief:
Protocol Section: NCT02498860