Hypertension Clinical Trial
Official title:
b. p. m Study (Beats Per Minute): Heart Rate Development Whilst Treating Patients With Hypertension With Concor or Concor Plus
The b.p.m study will be performed to gain the insight in the courses of illness and therapy in subjects, suffering from hypertension and that have elevated heart rate. This study will show that a therapy with bisoprolol (Concor/Concor PLUS) or any other blood pressure lowering (antihypertensive) drug lowers blood pressure (BP) and heart rate and increases the quality of subjects' life.
The b.p.m study measures heart rate development whilst treating subjects with hypertension
with Concor [bisoprolol] or Concor Plus [bisoprolol + hydrochlorothiazide (HCTZ)].
The objectives of this study are:
After 6 months of the therapy treatment, 60% of the subjects showed a heart rate ≥ 80
beats/min.
An improved quality of life information after 6 months of therapy treatment, collected by
asking standardised questions A decrease in systolic and diastolic BP after 6 months
presented significant differences Digital sphygmomanometers (BP measuring devices) will be
supplied in order to document the values of BP and heart rate. Blood pressure and heart rate
should be measured at least 2 times, ideally 4 times per day. Furthermore, every subject
will additionally receive a documentation sheet, where he/she will record the measurement
data. The documentation sheet will be a part of the improvement of the quality of life; it
can be removed and passed on.
Every subject will be explained how to use and handle the BP measuring device and the
importance of the documentation. The assessment of the quality of life must be made at the
beginning and at the end of 6 month therapy. Within the framework of the examination the
attending physician will ask 8 standard questions (SQ-8 Short Form Health Survey). The
questionnaire will be a part of the quality of life assessment.
The main focus of the observation is on the age group < 55 years with concomitant diseases,
such as diabetes or ketohexokinase (KHK).
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