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Clinical Trial Summary

The purpose of this research study is to determine the safety and feasibility of using the UroNav software and DynaCAD software for planning and treating prostate cancer as an add on to the already approved workflow of using ultrasound only during the cryoablation of the prostate. The software application may aid doctors in locating a prior biopsy proven cancer location from the UroNav biopsy that patients previously had and then use that information to guide the treatment.


Clinical Trial Description

This is a single-center, prospective, single arm study to evaluate feasibility of UroNAV Ablation system aided cryo-ablation treatment of low and intermediate risk, organ-confined prostate cancer. All subjects will be treated and then followed up clinically for up to 24 months to evaluate any procedure or device related adverse events as well as to assess efficacy endpoints of the study. Additional data related to quality of life of treated subjects will also be collected ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04656678
Study type Interventional
Source Northwell Health
Contact Ardeshir R Rastinehad, DO
Phone 212-434-6580
Email Arastine@northwell.edu
Status Recruiting
Phase N/A
Start date November 25, 2020
Completion date October 30, 2025

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