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Active, not recruiting Not applicable Interventional

A Comparison of TULSA Procedure vs. Radical Prostatectomy in Participants With Localized Prostate Cancer

ClinicalTrials.gov ID: NCT05027477

Public ClinicalTrials.gov record NCT05027477. 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 Jul 21, 2026, 10:59 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

Customized Ablation of the Prostate With the TULSA Procedure Against Radical Prostatectomy Treatment: a Randomized Controlled Trial for Localized Prostate Cancer (CAPTAIN)

Study identification

NCT ID
NCT05027477
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
Profound Medical Inc.
Other
Enrollment
201 participants

Conditions and interventions

Interventions

  • Radical Prostatectomy Device
  • TULSA Procedure Device

Device

Eligibility (public fields only)

Age range
40 Years to 80 Years
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
Oct 31, 2021
Primary completion
Aug 30, 2026
Completion
Aug 30, 2036
Last update posted
Aug 16, 2025

2021 – 2036

United States locations

U.S. sites
19
U.S. states
9
U.S. cities
17
Facility City State ZIP Site status
Arizona State Urological Institute Chandler Arizona 85224
East Valley Urological Center Mesa Arizona 85206
Investigate MD Scottsdale Arizona 85255
Atlantic Urology Medical Group Long Beach California 90806
Urology Group of Southern California Los Angeles California 90017
University of California, Los Angeles Los Angeles California 90024
Comprehensive Urology Medical Group Los Angeles California 90048
Alarcon Urology Center Montebello California 90640
Pasadena Urological Medical Group Pasadena California 91101
Stanford Cancer Center Stanford California 94305
Yale Cancer Center New Haven Connecticut 06511
Mayo Clinic Jacksonville Jacksonville Florida 32224
Sarasota Memorial Health Care System Sarasota Florida 34239
Indiana University Indianapolis Indiana 46202
Johns Hopkins School of Medicine Baltimore Maryland 21287
Mayo Clinic Rochester Minnesota 55905
Cleveland Clinic Cleveland Ohio 44106
The University of Texas Southwestern Medical Center Dallas Texas 75390-9020
The Urology Place San Antonio Texas 78240

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05027477, 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 Aug 16, 2025 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05027477 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →