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Clinical Trial Summary

This pilot study will establish non-invasive sample collections, including breath, saliva, blood and urine pre-surgery and at the participant's one-month post-surgery follow-up visit. Participants with suspected non-small cell lung cancer (NSCLC) stage I-III will be recruited.


Clinical Trial Description

Primary Objective - To evaluate the feasibility of adding non-invasive sample collections in the pre-surgical setting and at the post-surgery follow-up visit. - To identify and assess metabolic and microbial signatures collected at pre- and post-surgery and determine which are indicative of lung cancer. Secondary Objective - To identify signatures which are associated with lung cancer stage. - To identify signatures which are impacted by patient's pulmonary function status. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03998189
Study type Interventional
Source Wake Forest University Health Sciences
Contact
Status Terminated
Phase N/A
Start date October 11, 2019
Completion date June 21, 2021

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