Canadian Cohort of Convective Thermal Therapy Using Rezūm System in Benign Prostatic Hyperplasia (BPH).
Recruiting
- Conditions
- Urologic Diseases
- Interventions
- Procedure: Rezum
- Registration Number
- NCT05201131
- Lead Sponsor
- Can-Am HIFU Inc.
- Brief Summary
To document the clinical outcome of Rezūm therapy for BPH patient in Canadian cohort.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- Male
- Target Recruitment
- 50
Inclusion Criteria
- Male subjects of ≥ 18 years of age.
- Primary diagnosis of Benign Prostate Hypertrophy (BPH).
- Candidate for Rezūm therapy as per clinical decision of Investigator.
- Willing and able to accurately complete the required questionnaires.
- Willing and able to provide signed and dated informed consent
Exclusion Criteria
- Characteristics indicating a poor compliance with study protocol requirements.
- Disease or other health condition that is not suitable for this study.
- Unable or unwilling to provide signed informed consent.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Rezum procedure Rezum -
- Primary Outcome Measures
Name Time Method Maximum flow rate (Q-max) Baseline Maximum flow rate (Q-max)
Prostate Volume measured by transrectal ultrasound (TRUS) Baseline Prostate Volume measured by transrectal ultrasound (TRUS)
Questionnaire Baseline IPSS
Adverse Events Baseline Adverse Events
Change of Adverse Events 36 months after surgery Change of Adverse Events
Change of Post-Void Residual (PVR) volume 36 months after surgery Change of Post-Void Residual (PVR) volume
Change of Prostate Volume measured by transrectal ultrasound (TRUS) 12 months after surgery Change of Prostate Volume measured by transrectal ultrasound (TRUS)
Change of Maximum flow rate (Q-max) 36 months after surgery Change of Maximum flow rate (Q-max)
Post-Void Residual (PVR) volume Baseline Post-Void Residual (PVR) volume
Change of Questionnaire 36 months after surgery Change of IPSS score
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Dean Elterman
🇨🇦Toronto, Ontario, Canada