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Clinical Trial Summary

Twenty (20) subjects presenting with a hyperplasia enlarged prostate and candidates for surgery will undergo a single treatment for ablation of the prostate using the study device.Follow up visits are scheduled for the day of release from the hospital and at 1 and 3 months post procedure.

The primary objective of this study is to explore Vaporization efficacy and safety when treating PBH (Benign prostatic hyperplasia ) with the contact side firing fiber with recommended settings.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02683980
Study type Interventional
Source Lumenis Ltd.
Contact
Status Active, not recruiting
Phase N/A
Start date February 2016
Completion date September 2017