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Clinical Trial Summary

The SIBERIA study demonstrated a clear advantage of CGuard stent implantation over the existing classical stent when using a distal anti-embolic device. At the same time, there is no Level 1 evidence for a difference between the proximal and distal anti-embolic device for the CGuard stent.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05257161
Study type Interventional
Source Meshalkin Research Institute of Pathology of Circulation
Contact Andrey A Kaprenko, MD
Phone +79139504100
Email a_karpenko@meshalkin.ru
Status Recruiting
Phase N/A
Start date November 1, 2021
Completion date January 1, 2027

See also
  Status Clinical Trial Phase
Completed NCT03488199 - The SIBERIA Trial (Acculink™ Versus CGuard™) N/A