In Vivo Smart Biopsy Device Protocol In Radiology

Status Active, not recruiting

Clinical Trial Summary

This study is designed to demonstrate the feasibility of use of the Smart Biopsy Device in real clinical settings.

Clinical Trial Description

This is a single arm, multicenter study. It will be conducted in 3 medical centers, in the breast-imaging unit during ultrasonic guided core needle biopsy procedures performed in women with abnormality in the breast.

The study duration is only during the biopsy procedure, and the follow up period is 2 -3 weeks. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03914911
Study type	Interventional
Source	Dune Medical Devices
Contact
Status	Active, not recruiting
Phase	N/A
Start date	March 14, 2019
Completion date	March 31, 2020

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