ROSE for Improved Molecular Marker Testing Via EBUS

NAEnrolling by invitationINTERVENTIONAL
Enrollment

349

Participants

Timeline

Start Date

May 14, 2021

Primary Completion Date

December 31, 2025

Study Completion Date

March 1, 2026

Conditions
Non-small Cell Lung Cancer (NSCLC)
Interventions
OTHER

ROSE (presence of cytotech) & liquid prep

Standard of care EBUS will include presence of trained cytotechnologist providing on-site cytopathology feedback to bronchoscopist during the procedure. Sample is liquid.

OTHER

NO-ROSE (absence of cytotech) & liquid prep

Standard of care EBUS will NOT include presence of trained cytotechnologist providing on-site cytopathology feedback to bronchoscopist during the procedure. Sample is liquid.

OTHER

ROSE (presence of cytotech) & tissue clot sample

Standard of care EBUS will include presence of trained cytotechnologist providing on-site cytopathology feedback to bronchoscopist during the procedure. Sample is a tissue clot.

OTHER

NO-ROSE (absence of cytotech) & tissue clot sample

Standard of care EBUS will NOT include presence of trained cytotechnologist providing on-site cytopathology feedback to bronchoscopist during the procedure. Sample is a tissue clot.

Trial Locations (4)

21224

Johns Hopkins Bayview Medical Center, Baltimore

21287

Johns Hopkins Hospital, Baltimore

29425

The Medical University of South Carolina (MUSC), Charleston

60611

Northwestern Medicine, Chicago

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

AstraZeneca

INDUSTRY

lead

Johns Hopkins University

OTHER