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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 ongoing, but not recruiting participants.
Sponsor:
Information provided by (Responsible Party):
Tryton Medical, Inc.
ClinicalTrials.gov Identifier:
NCT01258972
First received: December 9, 2010
Last updated: November 11, 2015
Last verified: October 2015
No Study Results Posted on ClinicalTrials.gov for this Study
  Study Status: This study is ongoing, but not recruiting participants.
  Estimated Study Completion Date: July 2016
  Primary Completion Date: November 2012 (Final data collection date for primary outcome measure)
No publications provided by Tryton Medical, Inc.

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):