The study focuses on the development of a new personalized approach to diagnostics and surgical treatment of patients with ischemic cardiomyopathy. The algorithm for selection of patients for certain type of cardiac surgery will be developed. The models for prediction of the risks and outcomes of cardiac surgery will be elaborated to reduce the rate of complications in the early and long-term postoperative period in patients with ischemic cardiomyopathy. Imaging modalities, methods for assessement of structural and functional state of the myocardium, biochemistry testing, immunohistochemical examination, and myocardial biopsy studies will be used to achieve these goals.
The aim of the study is to develop a new personalized approach to diagnostics and surgical treatment of patients with ischemic cardiomyopathy.
Research Objectives:
Structured collection of patient data will be performed in a database formed on the platform of the Microsoft Excel 2010 software (Microsoft Corp., USA). Statistical processing of the results will be carried out using the SPSS 23.0 for Windows software package (IBM Corp., Armonk, NY, USA). The normality of the law of distribution of quantitative indicators will be checked using the Shapiro-Wilks criterion. Normally distributed parameters will be presented as mean value (M) and standard deviation (StD) in the form M StD; not normally distributed parameters will be presented as median (Me) and the 1st and 3rd interquantile intervals (Q25
Survival analysis will be performed using the Kaplan-Meier method. All statistics will be considered significant at p <0.05.
During the work, the methods of statistical analysis can be revised and (or) supplemented.
Condition | Chronic Heart Failure, cardiovascular diseases, Ischemic Cardiomyopathy, cardiovascular disorders, cardiovascular disease (cvd), cardiovascular system diseases, Cardiovascular Disease |
---|---|
Treatment | coronary artery bypass graft (CABG) with surgical ventricular restoration (SVR) and mitral repair (MR) |
Clinical Study Identifier | NCT04489355 |
Sponsor | Tomsk National Research Medical Center of the Russian Academy of Sciences |
Last Modified on | 15 October 2021 |
,
You have contacted , on
Your message has been sent to the study team at ,
You are contacting
Primary Contact
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
Learn moreEvery year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.
Sign up as volunteer
Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!
No annotations made yet
Congrats! You have your own personal workspace now.