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Clinical Trial Summary

The objective of this study is to evaluate the rate of SYNERGY 48 mm stent strut coverage and assess neointimal progression via OCT measurement in patients who underwent PCI.


Clinical Trial Description

Patients with stable, unstable angina and non-ST-elevation ACS will be included in this study. Patient will undergo coronary angiography for coronary anatomy assessment and estimation indications for PCI . After screening an OCT-guided PCI with extra long SYNERGY stent implantation will be provided in all patients. Patient will be divided into 2 groups of follow-up and will be followed within 3 and 6 month after procedure. Final clinical follow-up will be assessed at 12 month for all patients. At each follow-up visits the data regarding clinical events, coronary angiography and OCT-imaging will be collected. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03401216
Study type Interventional
Source Meshalkin Research Institute of Pathology of Circulation
Contact Aleksei Prokhorikhin, MD
Phone +79137178040
Email turbogold@list.ru
Status Recruiting
Phase N/A
Start date March 20, 2017
Completion date April 30, 2019

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