RecruitingNCT05001477

Customized TULSA-PRO Ablation Registry


Sponsor

Profound Medical Inc.

Enrollment

1,000 participants

Start Date

Oct 27, 2021

Study Type

OBSERVATIONAL

Conditions

Summary

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.


Eligibility

Sex: MALEMin Age: 18 Years

Inclusion Criteria4

  • Male
  • \>18 years old
  • Candidate for TULSA-PRO treatment
  • willing and able to sign the Informed Consent form

Exclusion Criteria1

  • None.

Interventions

DEVICETULSA Procedure

Transurethral ultrasound ablation procedure


Locations(5)

RadNet's Liberty Pacific West Hills Facility

West Hills, California, United States

Mayo Clinic Jacksonville

Jacksonville, Florida, United States

Wellspan Health

York, Pennsylvania, United States

University of Texas Southwestern Medical Center

Dallas, Texas, United States

Urology Place

San Antonio, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT05001477


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