A Study of the Safety and Efficacy of the VytronUS Low-Intensity Collimated Ultrasound Ablation System

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
VytronUS, Inc.
ClinicalTrials.gov Identifier:
NCT01900678
First received: July 9, 2013
Last updated: June 26, 2015
Last verified: June 2015
No Study Results Posted on ClinicalTrials.gov for this Study
  Study Status: This study has been completed.
  Study Completion Date: January 2015
  Primary Completion Date: January 2015 (Final data collection date for primary outcome measure)