The aim of the observational study is to ascertain the degree of blood pressure control in the early-morning hours after 8 weeks of treatment with Telmisartan/Telmisartan+Hydrochlorothiazide and during 44 weeks of follow-up, in patients with hypertension using home blood pressure measurements.
Study Type
OBSERVATIONAL
Enrollment
18,299
Boehringer Ingelheim Investigational Site
Boehringer Ingelheim Investigational Site, Belgium
Boehringer Ingelheim Investigational Site
Boehringer Ingelheim Investigational Site, Canada
Boehringer Ingelheim Investigational Site
Change from baseline in mean early morning systolic blood pressure, mean early morning diastolic blood pressure, and degree of control. (6:00 to 11:59), BP < 135/85 mmHg. (HBPM: mean of morning measurements).
Time frame: 217 Weeks
Clinical control (office BP), response rates, reduction in office cuff systolic and diastolic BP. Office BP control criteria: BP < 140/90 mmHg. Pulse rate, pulse pressure, discontinuations and tolerability.
Time frame: 217 Weeks
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Boehringer Ingelheim Investigational Site, Colombia
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Boehringer Ingelheim Investigational Site, Czechia
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Boehringer Ingelheim Investigational Site, Ecuador
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Boehringer Ingelheim Investigational Site, Indonesia
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Boehringer Ingelheim Investigational Site, Jordan
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Boehringer Ingelheim Investigational Site, Lebanon
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Boehringer Ingelheim Investigational Site, Mexico
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Boehringer Ingelheim Investigational Site, Turkey (Türkiye)
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