iNod™ Ultrasound-Guided Needle Biopsy System Study

Status Withdrawn

Clinical Trial Summary

The purpose of this study is to collect information on the iNod™ System's safety and ability to see the iNod™ biopsy needle in real-time in endobronchial lesions, peripheral lung nodules, or lung masses.

Clinical Trial Description

This post-market study intends to further demonstrate the ability and safety of the iNod™ Ultrasound Guidance System and iNod™ Ultrasound Biopsy needle to perform transbronchial needle biopsy of endobronchial lesions, peripheral lung nodules, or lung masses under real-time ultrasound visualization. This is a prospective, multi-center case series of standard of care peripheral lung nodule biopsy procedures with up to 115 subjects at up to 10 centers. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05804435
Study type	Interventional
Source	Boston Scientific Corporation
Contact
Status	Withdrawn
Phase	N/A
Start date	January 2025
Completion date	February 2027

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