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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
GroupInterventionDescription
Rezum procedureRezum-
Primary Outcome Measures
NameTimeMethod
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)

QuestionnaireBaseline

IPSS

Adverse EventsBaseline

Adverse Events

Change of Adverse Events36 months after surgery

Change of Adverse Events

Change of Post-Void Residual (PVR) volume36 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) volumeBaseline

Post-Void Residual (PVR) volume

Change of Questionnaire36 months after surgery

Change of IPSS score

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Dean Elterman

🇨🇦

Toronto, Ontario, Canada

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