University Medical Center Groningen
Groningen, 9700 RB, Netherlands
NCT Number: NCT01726049
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).
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Phase 3
Groningen, 9700 RB, Netherlands
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
Secondary objectives
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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
Time frame: baseline and 12 weeks
change of mean pulmonary artery pressure between baseline and 12 weeks measured by heart catheterisation
Time frame: baseline and 12 weeks
difference in change of VO2 max between baseline and 12 weeks between Sildenafil and placebo group
Time frame: baseline and 12 weeks
difference in change of cardiac output between baseline and 12 weeks between Sildenafil and Placebo group
Time frame: baseline and 12 weeks
Difference in change of wedge pressure between baseline and 12 weeks between Sildenafil group and Placebo group
Time frame: 12 weeks
University Medical Center Groningen
Other
Effects of Sildenafil on Pulmonary Arterial Pressure in Patients With Heart Failure With Preserved Ejection Fraction ( HFpEF) and Pulmonary Hypertension
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT05475028
Arrhythmias, Cardiac, Atrial Fibrillation
Naples, Italy
View Trial DetailsNCT01431313
Cardiovascular Diseases, Heart Diseases
Pittsburgh, Pennsylvania, United States
View Trial DetailsNCT00820352
Cardiovascular Diseases, Heart Diseases
Waidhofen an der Thaya, Lower Austria, Austria
View Trial DetailsNCT05887271
Body Weight, Cardiovascular Diseases
Leicester, Leicestershire, United Kingdom
View Trial Details