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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 Oct 18, 2026, 11:04 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 29, 2022 (Actual)
Primary completion
Aug 14, 2024 (Actual)
Completion
Aug 14, 2024 (Actual)
Last update posted
Jun 2, 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 2, 2026 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04972097 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →