The study is designed to evaluate the effect of treatment with Micardis/MicardisPlus on blood pressure and its ability to reduce different indicated cardiovascular risks. Further on, the study will evaluate the current antihypertensive treatment pattern in the daily practice among the patient population at increased cardiovascular risk.
Study Type
OBSERVATIONAL
Enrollment
211
Change From Baseline in Systolic Blood Pressure (SBP)
Time frame: Baseline to 3rd visit (4-10 months)
Change From Baseline in Diastolic Blood Pressure (DBP)
Time frame: Baseline to 3rd visit (4-10 months)
Change From Baseline in SCORE (10 Year Risk for Fatal Cardiovascular Event)
A 10 year risk of fatal cardiovascular disease (CVD) in populations at high risk. Minimum 0 percent risk to Maximum 47 percent risk.
Time frame: Baseline to 3rd visit (4-10 months)
Change From Baseline in Framingham CVD Risk Assessment Score
10-year risk for hard coronary heart disease (CHD) outcomes (Myocardial Infarction and coronary death), according to Framingham Heart Study, measured in percent. Low risk (10 or less CHD risk at 10 years), intermediate risk (10-20), high risk (20 or more).
Time frame: Baseline to 3rd visit (4-10 months)
Change From Baseline in Framingham Stroke Risk Assessment Score
The risk assessment tool using data from the Framingham Heart Study to estimate 10-year risk for stroke, measured in percent. Low risk (10 or less stroke risk at 10 years), intermediate risk (10-20), high risk (20 or more).
Time frame: Baseline to 3rd visit (4-10 months)
Change From Baseline in Risk Assessment According to ESH/ESC Guidelines
ESH is the European society of hypertension, and ESC is the European society of cardiology.
Time frame: Baseline to 3rd visit (4-10 months)
Pecentage of Patients That Achieved Target Blood Pressure (BP) Values According to ESH/ESC
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Boehringer Ingelheim Investigational Site 24
Brežice, Slovenia
Boehringer Ingelheim Investigational Site 2
Brežice, Slovenia
Boehringer Ingelheim Investigational Site 12
Celje, Slovenia
Boehringer Ingelheim Investigational Site 16
Celje, Slovenia
Boehringer Ingelheim Investigational Site 17
Celje, Slovenia
Boehringer Ingelheim Investigational Site 1
Celje, Slovenia
Boehringer Ingelheim Investigational Site 33
Celje, Slovenia
Boehringer Ingelheim Investigational Site 18
Golnik, Slovenia
Boehringer Ingelheim Investigational Site 23
Golnik, Slovenia
Boehringer Ingelheim Investigational Site 29
Golnik, Slovenia
...and 26 more locations
ESH/ESC a goal of treatment to be below values 130/80 mm/Hg for diabetic patients and below 140/90 mmHg for non-diabetic patients
Time frame: 3rd visit (4-10 months)
Additional Antihypertensive Treatment Pattern at Visit 3 (End of Study)
Participants may have taken more than one antihypertensive treatment, so the percentages will not add to 100 percent.
Time frame: 3rd visit (4-10 months)
Change in Heart Rate From Baseline to Study End
Time frame: Baseline to 3rd visit (4-10 months)
Number of Patients With Adverse Events (AE)
Time frame: 4-10 months
Number of Participants Not Completing Study
Number of participants discontinuing study early for given reason
Time frame: 3rd visit (4-10 months)