Prospective, Single Blind, Randomized Controlled Study to Evaluate the Safety & Effectiveness of the Tryton Side Branch Stent Used With DES in Treatment of de Novo Bifurcation Lesions in the Main Branch & Side Branch in Native Coronaries (TRYTON)

This study is currently recruiting participants. (see Contacts and Locations)
Verified September 2014 by Tryton Medical, Inc.
Sponsor:
Information provided by (Responsible Party):
Tryton Medical, Inc.
ClinicalTrials.gov Identifier:
NCT01258972
First received: December 9, 2010
Last updated: September 10, 2014
Last verified: September 2014
No Study Results Posted on ClinicalTrials.gov for this Study
  Study Status: This study is currently recruiting participants.
  Estimated Study Completion Date: March 2017
  Estimated Primary Completion Date: March 2015 (Final data collection date for primary outcome measure)