Viewing Study NCT06380361


Ignite Creation Date: 2025-12-24 @ 12:03 PM
Ignite Modification Date: 2026-01-01 @ 10:37 AM
Study NCT ID: NCT06380361
Status: RECRUITING
Last Update Posted: 2025-01-13
First Post: 2024-03-27
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: InvestigatioN of a Smart Probe for Lung lEsion Characterization Using Impedance Technology
Sponsor: Sensome
Organization:

Study Overview

Official Title: InvestigatioN of a Smart Probe for Lung lEsion Characterization Using Impedance Technology
Status: RECRUITING
Status Verified Date: 2025-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: INSPECT
Brief 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.
Detailed 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 Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: