Safety and Effectiveness of the Optilume® BPH Catheter System in a Post-Market Study
Recruiting
N/A
Interventional Study
Benign Prostatic Hyperplasia
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 50 and older
- Sex
- Male
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 92 (estimated)
- Sponsor
- Urotronic Inc. · Industry
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About This Trial
The goal of this clinical trial is to verify the continued safety and effectiveness for the Optilume BPH Catheter System.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
1. Male subject ≥ 50 years old
2. Diagnosed with lower urinary tract symptoms (LUTS) secondary to obstructive benign prostatic hyperplasia (BPH)
3. Able to be treated with the Optilume BPH Catheter System in accordance with the Instructions for Use
4. Prostate volume \< 80 g wit…