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It's a non-randomized, intervention, prospective, single-center study.
The aim of the work is to identify of biomarkers of unstable atherosclerosis in brachiocephalic arteries
Tasks:
Full description
The recruitment of patients will be carried out at the University Clinical Hospital No. 1 of Federal State Autonomous Educational Institution of Higher Education I.M. Sechenov First Moscow State Medical University of the Ministry of Health of the Russian Federation (Sechenov University). The study will include up to 50 people - the study group with atherosclerosis of the brachiocephalic arteries and up to 30 people - the control group without brachiocephalic atherosclerosis.
As part of the standard of medical care, the patient has already undergone and received the results of the following examinations before being included in the study:
Patients with clinically significant atherosclerosis of the brachiocephalic arteries were hospitalized for an operation - carotid endarterectomy with obtaining surgical material (atherosclerotic plaque with adjacent intima).
Specific methods of the planned study (procedures for examination and treatment of the patient):
During the operation according to the standard protocol of carotid endarterectomy, an atherosclerotic plaque with a small area of adjacent intima is removed. An atherosclerotic plaque obtained during a carotid endarterectomy will be sent for histological examination to determine signs of instability. The obtained data will be compared with the level of isolated microRNAs in blood and tissue (atherosclerotic plaque, intima) to detect microRNAs, which are determined during an unstable course of the atherosclerotic process.
The data obtained will make it possible to predict the unstable course of atherosclerosis using non-invasive studies. This will allow timely detection of unstable plaques and help to make a decision and determine the tactics of managing patients with borderline sizes of atherosclerotic lesions.
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Primary purpose
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Interventional model
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90 participants in 2 patient groups
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Central trial contact
Anastasiia Lomonosova, no; Philipp Kopylov, yes
Data sourced from clinicaltrials.gov
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