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Completed

NCT Number: NCT01726049

Sildenafil in HFpEF (Heart Failure With Preserved Ejection Fraction) and PH

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).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

University Medical Center Groningen

Groningen, 9700 RB, Netherlands

About this study

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

  • 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

  • To investigate whether Sildenafil treatment results in an reduction of wedge pressure in HFpEF patients.
  • To investigate whether Sildenafil treatment results in an improvenemt of cardiac output (CO) in HFpEF patients.
  • To investigate whether Sildenafil treatment results in improvement of exercise capacity in these patients ( defined as change in VO2max)

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • >18 years
  • Written inform consent
  • PH secondary to diastolic left heart failure defined as
  • PAP mean >25 mmHg
  • Wedge mean >15 mmHg
  • Normal systolic left ventricular (LV) function on echo/nuclear imaging (left ventricular ejection fraction (LVEF) > or =45%)
  • New York Heart Association class (NYHA) II-IV despite heart failure therapy

Exclusion criteria

  • Severe noncardiac limitation to exercise (as severe chronic obstructive pulmonary disease)
  • Other cause of PH besides diastolic heart failure
  • Coronary ischemia or recent myocardial infarction (<6 months)
  • Hypotension ( <90/50 mmHg)
  • Ongoing nitrate therapy
  • Ongoing therapy with citochrome P450 3A4 ( CYP3A4) inhibitors (ketoconazole, erythromycin, cimetidine, clarithromycin, itraconazole, voriconazole and protease inhibitors) or CYP3A4 inductors(carbamacepine, phenytoin, phenobarbital, rifampicin, Sint Janskruid ). Furthermore patients will be informed not to drink grapefruit juice while on study medication because of the known impact of grape fruit on pharmacokinetics of Sildenafil.
  • Ongoing therapy with alpha -inhibitors
  • Significant mitral or aortic valve dysfunction
  • Severe liver dysfunction
  • Pregnancy
  • Unable to read and comprehend Dutch language

Treatment and study plan

Sildenafil

Drug

Sildenafil administered orally 3 times per day 20 mg for the first 2 weeks, followed by 3 times 60 mg for 10 weeks

Placebo

Drug

Placebo tablets 3 times per day 20 mg foor de first 2 weeks, followed by 3 times 60 mg for 10 weeks

Primary outcomes

  1. Mean Pulmonary Artery Pressure Measured by Right Heart Catheterization

    Time frame: baseline and 12 weeks

    change of mean pulmonary artery pressure between baseline and 12 weeks measured by heart catheterisation

Secondary outcomes

  1. VO2max

    Time frame: baseline and 12 weeks

    difference in change of VO2 max between baseline and 12 weeks between Sildenafil and placebo group

  2. Cardiac Output Measured Invasively by Right Heart Catheterization

    Time frame: baseline and 12 weeks

    difference in change of cardiac output between baseline and 12 weeks between Sildenafil and Placebo group

  3. Wedge Pressure Measured Invasively by Right Heart Catheterization

    Time frame: baseline and 12 weeks

    Difference in change of wedge pressure between baseline and 12 weeks between Sildenafil group and Placebo group

Other outcomes

  1. Echocardiographic Parameters of Diastolic LV Dysfunction

    Time frame: 12 weeks

Sponsors and collaborators

Lead sponsor

University Medical Center Groningen

Other

Collaborators

  • Pfizer

Registry information

Official study title

Effects of Sildenafil on Pulmonary Arterial Pressure in Patients With Heart Failure With Preserved Ejection Fraction ( HFpEF) and Pulmonary Hypertension

Important dates

Study start
2011
Primary completion
2014
Study completion
2014
First posted
Nov 14, 2012
Registry last updated
Mar 21, 2016

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.

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