Aim of the study is to investigate whether Sildenafil treatment results in a reduction of pulmonary artery pressure without decrease of cardiac output (CO) and in improvement of exercise capacity in patients with heart failure with preserved ejection fraction (HFpEF) with pulmonary hypertension ( PH).
Rationale: Treatment of diastolic left heart failure is a challenging task. Compared to systolic left heart failure the level of evidence for known medical treatment regiments is low. Sildenafil, a phosphodiesterase 5 (PDE 5) inhibitor and effective therapy for pulmonary arterial hypertension acts as a selective pulmonary vasodilator by inhibiting the impaired nitric oxide (NO) pathway. Reducing the pulmonary vascular resistance would be the primary target by treatment of diastolic left heart failure with PH. But clinical and hemodynamical studies to evaluate the role of Sildenafil in diastolic heart failure, also called heart failure with preserved ejection fraction (HFpEF) with secondary pulmonary hypertension are lacking. Our hypothesis is that Sildenafil decreases pulmonary artery pressure in patients with HFpEF and pulmonary hypertension. Objective: To investigate whether Sildenafil treatment results in a hemodynamic improvement and in an improvement of exercise capacity in these patients. Study design: single-center, prospective, randomized, placebo controlled study. Study population: 52 patients with HFpEF and PH Intervention : One group receives three times daily 20 mg Sildenafil for 2 weeks followed by three times daily 60 mg Sildenafil for 10 weeks. The other group receives three times daily 20 mg of Placebo, followed by 3 times daily 60 mg placebo. Main study parameters/endpoints: Primary objectives 1\. To investigate whether Sildenafil treatment results in a reduction of pulmonary artery pressure (PAP) in HFpEF patients with PH (investigated invasively by right heart catheterization) . Secondary objectives 1. To investigate whether Sildenafil treatment results in an reduction of wedge pressure in HFpEF patients. 2. To investigate whether Sildenafil treatment results in an improvenemt of cardiac output (CO) in HFpEF patients. 3. To investigate whether Sildenafil treatment results in improvement of exercise capacity in these patients ( defined as change in VO2max)
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
52
Sildenafil administered orally 3 times per day 20 mg for the first 2 weeks, followed by 3 times 60 mg for 10 weeks
Placebo tablets 3 times per day 20 mg foor de first 2 weeks, followed by 3 times 60 mg for 10 weeks
University Medical Center Groningen
Groningen, Netherlands
Mean Pulmonary Artery Pressure Measured by Right Heart Catheterization
change of mean pulmonary artery pressure between baseline and 12 weeks measured by heart catheterisation
Time frame: baseline and 12 weeks
VO2max
difference in change of VO2 max between baseline and 12 weeks between Sildenafil and placebo group
Time frame: baseline and 12 weeks
Cardiac Output Measured Invasively by Right Heart Catheterization
difference in change of cardiac output between baseline and 12 weeks between Sildenafil and Placebo group
Time frame: baseline and 12 weeks
Wedge Pressure Measured Invasively by Right Heart Catheterization
Difference in change of wedge pressure between baseline and 12 weeks between Sildenafil group and Placebo group
Time frame: baseline and 12 weeks
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