Clinical Trial

The LungVision Navigational Platform for Preoperative Labeling of Pulmonary Ground Glass Nodules With Fiducial Markers

Recruiting
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Record status
This record was last updated September 18, 2025 (before its estimated January 1, 2026 completion). Its status may not reflect the trial's current state.
Summary
Based on current evidence, there are no studies investigating the possibility of placing a fiducial marker using augmented fluoroscopy, particularly for partially solid lesions that are often not visible on traditional fluoroscopy. The study in question could provide evidence that will allow, in the future, the use of the LungVision system and radial ultrasound to effectively mark a lesion with a ground glass component highly suspected of malignancy via bronchoscopy, avoiding more invasive marking procedures such as trans-thoracic marking. Correct marking of the target lesion will allow easy identification of the lesion during surgery and its complete removal through small resections, obtaining a definitive histological diagnosis and, in some cases, radical oncological treatment with preservation of healthy lung tissue.
Trial Details
NCT Number NCT07180823
Lead Sponsor IRCCS Azienda Ospedaliero-Universitaria di Bologna
Conditions Lung Cancer
Enrollment 5 participants
Start Date 2025-07-21
Primary Completion 2026-01-01 (estimated)
Study Completion 2026-02-28 (estimated)
Updated on ClinicalTrials.gov 2025-09-18