Condition: Patients With Aterosclerotic Carotid Stenosis · Symptomatic Patients (Stenosis > 50%) · Asymptomatic Patients (Stenosis ≥80%) · Sponsor: Meshalkin Research Institute of Pathology of Circulation
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.
This description comes directly from the study's public registry record.
Andrey A Kaprenko, MD · +79139504100 · a_karpenko@meshalkin.ru
Always discuss trial participation with your own doctor first.
| E. Meshalkin National Medical Research Center | Novosibirsk, Russia | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05257161