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Clinical Trial Summary

The objective of the study is to evaluate the feasibility of the BioSpy System sensor to differentiate tissues that are encountered during bronchoscopic biopsy of endobronchial tumors and peripheral lung nodules and masses.


Clinical Trial Description

Participants in this study require a lung biopsy to confirm if they have a lung tumour. A biopsy is a procedure where a piece of lung tissue is removed for testing. Current biopsy techniques cannot guarantee the exact location of lung tumours, so biopsies can be taken from healthy tissue. The BioSpy System (BSS) is a device with a probe, which is placed inside a normal biopsy needle. The tip of the probe contains sensors, that will scan the composition of the tissue which is in contact with the sensors. The INSPECT study aims at collecting the sensor data, with the goal of being able to differentiate the different tissues. All study participants will have a biopsy with the BSS. Participants will have a hospital visit for the procedure, and will have to stay up to 16 hours after their procedure as per normal hospital practice. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06380361
Study type Interventional
Source Sensome
Contact Julie Lafaurie, PhD
Phone + 33 1 85 37 07 70
Email julie@sensome.com
Status Recruiting
Phase N/A
Start date March 28, 2024
Completion date April 1, 2025

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