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Clinical Trial Summary

The purpose of this study is to evaluate the safety and effectiveness of using UroLift in subjects with a prostatic median lobe enlargement due to benign prostatic hyperplasia (BPH).


Clinical Trial Description

Study Objectives: Evaluate the safety and effectiveness of the UroLift® System when used in symptomatic benign prostatic hyperplasia (BPH) subjects with an enlarged median lobe.

Study Design: Prospective, multicenter, non-blinded, single arm (non-randomized) study.

Sample Size: A total of no more than 48 subjects will be enrolled. Subject Population: Males age of 50 years or older diagnosed with lower urinary tract symptoms (LUTS) with enlarged median lobe. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02625545
Study type Interventional
Source NeoTract, Inc.
Contact
Status Completed
Phase N/A
Start date February 17, 2016
Completion date December 19, 2017

See also
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