METHOD is a prospective observational program that will be conducted in 1centre of the Russian Federation. Prospective follow-up will be for about 6 months. The METHOD study is a 2 visit study with first visit of inclusion and second visit of completion of the study. Patients with stable angina pectoris eligible to the study inclusion criteria will be invited to participate in this observational program. The parameters for analysis will be collected by doctors and entered into CRF. The final analysis will include data from patients who were taking TMZ 80 mg OD during the observational period. The decision to stop the study will be made once 36 patients receiving treatment with trimetazidine 80 mg OD will have been evaluated at V1. It is expected that 5 cardiologists will participate in the program. The planned number of patients is 36.
To describe antiischemic and antianginal effectiveness of trimetazidine OD 80 mg as well as adherence to the treatment with TMZ 80 mg OD in patients with stable angina pectoris and prior MI in real clinical practice in Russia
Study Type
OBSERVATIONAL
Enrollment
36
speckle tracking mode of the stress ECHO test with dobutamine
"Institute for Complex Issues of Cardiovascular Diseases"
Kemerovo, Russia
Barbarash Olga Leonidovna
Moscow, Russia
To describe antiischemic effectiveness of TMZ 80 mg OD assessed by the speckle tracking mode of the stress ECHO test with dobutamine in patients included in the study.
Time frame: 6 months
To describe antianginal effectiveness of TMZ 80 mg OD in patients included in the study
Time frame: 6 months
To describe adherence to TMZ 80 mg OD in patients included in the study;
Time frame: 6 months
To describe correlations between adherence (low, medium or high) to the treatment with TMZ 80 mg OD and antiischemic and antianginal effectiveness of TMZ 80 mg OD in patients included in the study;
Time frame: 6 months
To describe impact on quality of life (QoL) to the treatment with TMZ 80 mg OD
Time frame: 6 months
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