Customized TULSA-PRO Ablation Registry
Recruiting · NCT05001477 · Observational (researchers observe without assigning treatment) · Lead sponsor: Profound Medical Inc.
View the official record on ClinicalTrials.gov →Interventions studied
TULSA Procedure
What this trial is about
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.
Who can take part
Age range
18 Years and older
Sex
Male
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
Inclusion criteria
- Male
- \>18 years old
- Candidate for TULSA-PRO treatment
- willing and able to sign the Informed Consent form
Exclusion criteria
- None.
Where it is running
5 locations listed across 4 US states.
- 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