Description Module

Description Module

The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.

Description Module path is as follows:

Study -> Protocol Section -> Description Module

Description Module


Ignite Creation Date: 2025-12-25 @ 2:41 AM
Ignite Modification Date: 2025-12-25 @ 2:41 AM
NCT ID: NCT05714033
Brief Summary: To learn if LADS is better than VESPA at preventing atelectasis during a robotic bronchoscopy.
Detailed Description: Primary Objective: To compare the proportion of patients developing target-obscuring atelectasis when using a lateral decubitus strategy (LADS) vs using a ventilatory strategy to prevent atelectasis (VESPA) during robotic bronchoscopy for posteriorly-located peripheral lung lesions. Secondary Objectives: * To compare the proportion of patients with atelectasis in the target lobe in VESPA vs. LADS during robotic bronchoscopy. * To compare the proportion of patients with atelectasis obscuring 100%, 50% or more, and less than 50% of the target during robotic bronchoscopy using LADS vs. VESPA. * To compare the proportion of patients in whom a biopsy sample was not taken due to atelectasis using LADS vs. VESPA. * To compare the diagnostic yield using LADS vs. VESPA. * To compare the proportion of tool in lesion (TIL) using LADS vs. VESPA. * To compare the diagnostic accuracy (sensitivity and specificity) for malignancy using LADS vs. VESPA. * To compare the proportion of LADS-induced vs. VESPA-induced complications. * To compare the proportion of bronchoscopy-induced complications in LADS vs. VESPA. * To compare the accuracy of 3D-2D image registration using LADS vs. VESPA. * To compare clinical workflow in robotic bronchoscopy with VESPA and LADS strategies to identify potential improvements in workflow.
Study: NCT05714033
Study Brief:
Protocol Section: NCT05714033