Previous studies have demonstrated a direct association between blood pressure level and cardiovascular risk. However in patients with heart failure this association is considered controversial. The aim of this study is to evaluate the effect of the reduction of blood pressure in patients with heart failure. The investigators will examine the effects of this intervention over mortality, quality of life, and cardiac function.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
21
Patients will receive drug therapy aimed to reducing blood pressure - first line drug will be hydralazine up to 100mg/day; if systolic blood pressure reduces less than 20% from baseline and remains over 100mmHg patients will further receive amlodipine up to 10mg/day
Patients will receive placebo
Heart Institute (InCor) do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
São Paulo, São Paulo, Brazil
Any cause mortality
Time frame: 12 months after randomization
Unplanned hospital admission from any cause
Time frame: 12 months after randomization
Cardiovascular death
Time frame: 12 months after randomization
Acute myocardial ischemia
Time frame: 12 months after randomization
Stroke
Time frame: 12 months after randomization
Symptomatic hypotension
Time frame: 12 months after randomization
Renal function
Time frame: 12 months after randomization
Peak exercise oxygen consumption
Time frame: 12 months after randomization
Quality of life
Time frame: 12 months after randomization
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