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UroLift System TOlerability and ReCovery When Administering Local Anesthesia — LOCAL  

Benign Prostatic Hyperplasia Clinical Trial

Official title:
L.O.C.A.L. Study -- UroLift System TOlerability and ReCovery When Administering Local Anesthesia

Clinical Trial Summary

The purpose of the study is to evaluate procedure tolerability and surgical recovery following the UroLift® system procedure when conducted with local anesthesia in subjects with symptomatic benign hyperplasia (BPH). Primary effectiveness will be achieved by looking at the Quality of Recovery Visual Analog Scale (QoR VAS) by the one month follow-up visit.

Clinical Trial Description

The randomized portion of the study is a prospective, multicenter, non-blinded, single arm trial evaluating procedure tolerability and surgical recovery following the UroLift® system procedure when conducted with local anesthesia. All subjects undergo UroLift system treatment and will be followed through 5 years after receiving the investigational device. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01876706
Study type Interventional
Source NeoTract, Inc.
Contact
Status Completed
Phase N/A
Start date April 2013
Completion date September 4, 2018
View Details
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