The antihypertensive effect, safety and usefulness of treatment with BIBR 277 capsules were evaluated in hypertensive patients with nephropathy
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
23
Changes from baseline in hypertensive effect by investigator, using a 5-grade classification
Time frame: 8 weeks after start of treatment
Changes from baseline in blood pressure reduction
Time frame: 8 weeks after start of treatment
Rate of blood pressure normalisation
percentage of patients with \< 150/90 mmHg
Time frame: 8 weeks after start of treatment
Changes from baseline in blood pressure / pulse rate
Time frame: 8 weeks after start of treatment
Usefulness assessment by investigator, using a 5- grade classification
Time frame: 8 weeks after start of treatment
Overall safety assessment by investigator, using a 5- grade classification
Time frame: 8 weeks after start of treatment
Number of patients with adverse events
Time frame: Up to 12 weeks
Number of patients with abnormal changes in laboratory values
Time frame: Up to 8 weeks after start of treatment
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