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Active, not recruiting Not applicable Interventional

Water Vapor Ablation for Localized Intermediate Risk Prostate Cancer

ClinicalTrials.gov ID: NCT05683691

Public ClinicalTrials.gov record NCT05683691. 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 Jun 25, 2026, 6:40 PM EDT

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

Official title

Prospective, Multicenter, Single-Arm Study of VanquishTM Water Vapor Ablation for PrOstate CanceR

Study identification

NCT ID
NCT05683691
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
Francis Medical Inc.
Industry
Enrollment
400 participants

Conditions and interventions

Interventions

  • Vanquish System Device

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
May 15, 2023
Primary completion
Mar 31, 2027
Completion
Mar 31, 2029
Last update posted
Jun 14, 2026

2023 – 2029

United States locations

U.S. sites
25
U.S. states
16
U.S. cities
23
Facility City State ZIP Site status
Mayo Clinic- Phoenix Phoenix Arizona 85054
Memorial Care Laguna Hills California 92653
University of Southern California Los Angeles California 90089
Kasraeian Urology Jacksonville Florida 32216
University of Chicago Chicago Illinois 60637
Wichita Urology Wichita Kansas 67226
Chesapeake Urology Baltimore Maryland 21204
Johns Hopkins Baltimore Maryland 21287
Corewell Health / William Beaumont University Hospital Royal Oak Michigan 48073
Michigan Institute of Urology Troy Michigan 48084
University of Minnesota Minneapolis Minnesota 55454
Mayo Clinic- Rochester Rochester Minnesota 55905
Minnesota Urology Woodbury Minnesota 55125
NYU Langone Health New York New York 10016
Northwell Health- Lenox Hill Hospital New York New York 11222
University of Rochester Rochester New York 14620
Duke Cancer Institute Durham North Carolina 27710
The Urology Group Cincinnati Ohio 45212
MidLantic Urology Bala-Cynwyd Pennsylvania 19004
Carolina Urologic Research Center Myrtle Beach South Carolina 29572
Urology Austin Austin Texas 78745
Houston Methodist Hospital and Research Institute Houston Texas 77030
The Urology Place San Antonio Texas 78240
Urology of Virginia, PLLC Virginia Beach Virginia 23462
Medical College of Wisconsin Milwaukee Wisconsin 53226

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 NCT05683691, 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 14, 2026 · Synced Jun 25, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05683691 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →