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Completed Not applicable Interventional Results available

Pivotal Study of the NanoKnife System for the Ablation of Prostate Tissue

ClinicalTrials.gov ID: NCT04972097

Public ClinicalTrials.gov record NCT04972097. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 2:42 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Pivotal Study of the NanoKnife System for the Ablation of Prostate Tissue in an Intermediate-Risk Patient Population

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Pivotal study to evaluate the use of the NanoKnife System as a focal therapy option for prostate cancer patients. This study will assess the safety and effectiveness of the device when used to ablate prostate tissue in intermediate-risk prostate cancer patients.

Study identification

NCT ID
NCT04972097
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Angiodynamics, Inc.
Industry
Enrollment
121 participants

Conditions and interventions

Interventions

Device

Eligibility (public fields only)

Age range
50 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 28, 2022
Primary completion
Aug 13, 2024
Completion
Aug 13, 2024
Last update posted
Jun 1, 2026

2022 – 2024

United States locations

U.S. sites
17
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
University of California Irvine Orange California 92868
University of Colorado Aurora Colorado 80045
University of Florida Health Gainesville Florida 32610
Moffitt Cancer Center Tampa Florida 33612
Rush University Medical Center Chicago Illinois 60612
Northshore University Healthsystem Evanston Illinois 60201
Duly Health and Care Lisle Illinois 60532
VA Ann Arbor Health Care Ann Arbor Michigan 48105
Mayo Clinic Rochester Minnesota 55905
NYU Langone Health New York New York 10017
Northwell Health New York New York 10022
Memorial Sloan Kettering Cancer Center New York New York 10065
Weill Cornell Medicine New York New York 10065
Duke University Durham North Carolina 27710
University of Cincinnati Cincinnati Ohio 45221
Fox Chase Cancer Center Philadelphia Pennsylvania 19111
University of Texas Southwestern Medical Center Dallas Texas 75390

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04972097, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 1, 2026 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04972097 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →