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 @ 1:06 AM
Ignite Modification Date:
2025-12-25 @ 1:06 AM
NCT ID:
NCT01473693
Eligibility Criteria:
Inclusion Criteria:
* Patients between the ages of 18 and 80 years old
* As per self report and/or medical record female patients are either postmenopausal or not able to become pregnant
* Patients with biopsy proven or suspected non-small cell lung cancer planned to undergo induction chemotherapy and surgery, OR with biopsy proven or suspected non-small cell lung cancer planned to undergo immediate surgical resection
* No clinical/neurological symptoms suggestive of brain metastases by attending's judgment as documented in the medical record and/or correspondence with the research team
* In the judgement of the consenting professional, patient is able to understand English, through verbal and written communication
* Patient is able to undergo MRI scanning (verified with pre-MRI Safety Screening form (Appendix A) used in MSKCC MRI Centers) completed at screening and again prior to having the MRI.
Exclusion Criteria:
* Patients with history of significant neurological diagnoses including stroke, tumor, dementia, epilepsy, or multiple sclerosis as indicated by medical records and/or self report
* History of head injury with evidence of brain injury or loss of consciousness for \> 60 minutes as per EMR or self-report
* No prior treatment with chemotherapy
* Participant has dentures, body jewelry or wig that they are unable to remove as per self-report
* Patient reports that he/she cannot undergo MRI scanning without significant distress or discomfort
* Significant psychiatric or cognitive disturbance sufficient, in the investigator's judgment, to preclude providing informed consent or participating in the study (i.e., schizophrenia).
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
80 Years
Study:
NCT01473693
Study Brief:
Protocol Section:
NCT01473693