About this trial
It is a prospective, controlled, single-center, observational, non-randomized study. The study is planned to include at least 4000 patients 18 years old and older in the training sample and 1000 patients over 18 years old in the test sample (the total number of patients is at least 5000 people). Patients will be included in the study if they have undergone a full examination (laboratory, clinical and instrumental), allowing for the verification or exclusion of cardiac and cardiac-associated pathology in accordance with current recommendations. During the course of the study, the authors of the work do not interfere with the above-mentioned scope of the examination, which is carried out on patients in accordance with clinical guidelines. All patients included in the study will undergo ECG recording in standard lead I for 1 minute twice, followed by spectral analysis of the obtained data, which will be stored at the remote monitoring center of Sechenov University without being linked to the personal data of patients. A spectral analysis of the electrocardiogram will be performed using a continuous wavelet transform. The result of this study will be the identification of ECG parameters that will correlate with cardiac and cardiac-associated pathology
Eligibility criteria
Qualifiers
The presence of written informed consent of the patient to participate in the study
Availability of examination data allowing for the verification or exclusion of cardiac and cardiac-associated pathology
Age 18 years old and older
Patients with an implanted permanent pacemaker;
Disqualifiers
Poor quality of the ECG recording on a single-channel ECG monitor
Insufficient examination data to verify or exclude cardiac or cardiac-associated pathology;
Patient's unwillingness to continue participating in the study for any reason.
Trial design
Treatments tested in this trial
- Not listed