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Clinical Trial Summary

In this monocentric randomized controlled trial, 120 potential non small cell lung cancer (NSCLC) patients for which tissue diagnosis and material for next generation sequencing (NGS) is required for clinical management will be approached the day of their endobronchial ultrasound to participate in the study. They will be randomized to 2 vs 3 passes/lymph node and will all undergo liquid biopsy. The co-primary outcomes are 1)the rate of obtention of adequate material for NGS testing with 2 vs 3 passes/lymph node and 2)the percentage of patients for which liquid biopsy allows to identify clinically pertinent findings not available from tissue biopsy


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05560776
Study type Interventional
Source Institut universitaire de cardiologie et de pneumologie de Québec, University Laval
Contact Marc Fortin, MD
Phone 4186568711
Email marc.fortin@criucpq.ulaval.ca
Status Not yet recruiting
Phase N/A
Start date November 1, 2022
Completion date February 1, 2025

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