ACTRN12613000167763
Active, not recruiting
未知
Single-arm prospective, interventional pilot study to evaluate the safety, feasibility and efficacy of the PROCEPT AquablationTM System (PAS) device for the treatment of Benign Prostatic Hyperplasia (BPH)
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- PROCEPT BioRobotics Corporation
- Enrollment
- 30
- Status
- Active, not recruiting
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Male, Age \> 50 years with BPH and history of inadequate response to medical therapy.
Exclusion Criteria
- •Large median lobe, urethral length \>6cm, prostates \>80g, prostate cancer, current urological conditions affecting procedural outcomes, previous prostate surgery, significant renal impairment, listed concomitant medications and listed uncontrolled co\-morbidities.
Outcomes
Primary Outcomes
Not specified
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