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Assess Safety and Performance of the Kronos Electrocautery Device for Electrocautery Procedures Following Coaxial Biopsy Procedures

Renal Disease Clinical Trial

Official title:
Feasibility Study of the Kronos Electrocautery Device

Clinical Trial Summary

The primary objective for this study is to assess safety and performance of the Kronos Electrocautery Device for electrocautery procedures following coaxial biopsy procedures on areas that include, but are not limited to, liver, kidney, lungs, breasts, soft tissue, etc.

Clinical Trial Description

The Kronos Electrocautery Device is intended to be used in electrocautery procedures to control bleeding by use of electrical current to heat the device probe tip that is applied directly to the target tissue area of treatment. Prospective, multi-center, single-arm study with consecutive, eligible subject enrollment at each site. Patients who require a coaxial biopsy procedures on areas that include, but are not limited to, liver, kidney, lungs, breasts, soft tissue, etc., will be eligible to participate in this study. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05593211
Study type Interventional
Source Single Pass Inc
Contact
Status Completed
Phase N/A
Start date October 17, 2022
Completion date February 9, 2023
View Details
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