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.
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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…
Contacts

Kaitlyn Palm

612-816-0068

kpalm@laborie.com

CONTACT

Steve Madej

smadej@laborie.com

CONTACT