Customized TULSA-PRO Ablation Registry

Part of paid clinical trials in West Hills, California.

Sponsor
Profound Medical Inc.
Study ID
NCT05001477
Status
Recruiting

Conditions

Eligibility Criteria

Sex
MALE
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • TULSA Procedure — DEVICE
    Transurethral ultrasound ablation procedure

Study Details

This patient registry will capture data from patients who have been or who are undergoing the transurethral ultrasound ablation (TULSA) procedure as part of their routine clinical care. The registry will shed light on real-world outcomes of safety and efficacy of the procedure and understand how a patient's quality of life is affected throughout their follow-up and lifetime.

Key Dates

Start date
Oct 27, 2021
Status verified
Nov 2023
Primary completion
Oct 31, 2026
Completion
Oct 31, 2061

Study Design

Enrollment
1,000 participants (estimated)

Primary Outcome Measure

Rate of complications [ Time Frame: 5 years ]

Central Contacts

Locations (5)

FacilityCityStateZIPSite coordinators
RadNet's Liberty Pacific West Hills FacilityWest HillsCalifornia91307
Kristi Maya
562-981-6101
Rachel Francisco Danas
562-459-3541
Robert Princenthal, MD (PRINCIPAL_INVESTIGATOR)
Martin Cohen, MD (SUB_INVESTIGATOR)
Mayo Clinic JacksonvilleJacksonvilleFlorida32224
Ann Dunshee
904-953-5102
Chandler Dora, MD (PRINCIPAL_INVESTIGATOR)
Wellspan HealthYorkPennsylvania17403
Sherrie Keller
717-741-8042
Edward Steiner, MD (PRINCIPAL_INVESTIGATOR)
University of Texas Southwestern Medical CenterDallasTexas75390
Anna Manning-Mortimer
904-953-5102
Daniel Costa, MD (PRINCIPAL_INVESTIGATOR)
Urology PlaceSan AntonioTexas78240
Victoria Sarwan
210-617-3670
Naveen Kella, MD
210-617-3670
Naveen Kella, MD (PRINCIPAL_INVESTIGATOR)

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