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 @ 12:32 AM
Ignite Modification Date: 2025-12-25 @ 12:32 AM
NCT ID: NCT02492867
Eligibility Criteria: Inclusion Criteria: * Patients must have FDG-avid and pathologically proven Stage IIA-IIIB non-small cell lung cancer. * Patients must be considered unresectable or inoperable. * Patients must be 18 years of age or older. * Patients must have a Karnofsky performance (A measure general well-being and activities of daily life. Scores range between 0 and 100 where 100 represents normal and 0 represents death.) of score \> or = to 70. * Patients must have adequate organ and marrow function. * Patient must be willing to use effective contraception if female with reproductive capability. * Patients must be informed of the investigational nature of this study and given written informed consent in accordance with institutional and federal guidelines. Exclusion Criteria: * Patients with any component of small cell lung carcinoma * Patients with evidence of a malignant pleural or pericardial effusion * Prior radiotherapy to the thorax such that composite radiation would significantly overdose critical structures, either per estimation of the treating radiation oncologist or defined by failure to meet normal tissue tolerance constraints * Patients cannot tolerate concurrent chemotherapy * Pregnant women are excluded from this study because radiation has the potential for teratogenic or abortifacient effects. * Prisoners are excluded for this study.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT02492867
Study Brief:
Protocol Section: NCT02492867