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

Primary Purpose

Heart Failure, Diastolic, Pulmonary Hypertension

Status
Completed
Phase
Phase 3
Locations
Netherlands
Study Type
Interventional
Intervention
Sildenafil
Placebo
Sponsored by
University Medical Center Groningen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure, Diastolic focused on measuring HFpEF, PH

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • University Medical Center Groningen

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Sildenafil

Placebo

Arm Description

Sildenafil orally 3 times 20mg for 2 weeks , followed by 3 times 60 mg for 10 weeks

placebo orally 3 times 20mg tablets, followed by 3 times 60 mg for 10 weeks

Outcomes

Primary Outcome Measures

Mean Pulmonary Artery Pressure Measured by Right Heart Catheterization
change of mean pulmonary artery pressure between baseline and 12 weeks measured by heart catheterisation

Secondary Outcome Measures

VO2max
difference in change of VO2 max between baseline and 12 weeks between Sildenafil and placebo group
Cardiac Output Measured Invasively by Right Heart Catheterization
difference in change of cardiac output between baseline and 12 weeks between Sildenafil and Placebo group
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

Full Information

First Posted
September 21, 2012
Last Updated
February 20, 2016
Sponsor
University Medical Center Groningen
Collaborators
Pfizer
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1. Study Identification

Unique Protocol Identification Number
NCT01726049
Brief Title
Sildenafil in HFpEF (Heart Failure With Preserved Ejection Fraction) and PH
Official Title
Effects of Sildenafil on Pulmonary Arterial Pressure in Patients With Heart Failure With Preserved Ejection Fraction ( HFpEF) and Pulmonary Hypertension
Study Type
Interventional

2. Study Status

Record Verification Date
February 2016
Overall Recruitment Status
Completed
Study Start Date
October 2011 (undefined)
Primary Completion Date
September 2014 (Actual)
Study Completion Date
December 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Medical Center Groningen
Collaborators
Pfizer

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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).
Detailed Description
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 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)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure, Diastolic, Pulmonary Hypertension
Keywords
HFpEF, PH

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
52 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sildenafil
Arm Type
Active Comparator
Arm Description
Sildenafil orally 3 times 20mg for 2 weeks , followed by 3 times 60 mg for 10 weeks
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
placebo orally 3 times 20mg tablets, followed by 3 times 60 mg for 10 weeks
Intervention Type
Drug
Intervention Name(s)
Sildenafil
Intervention Description
Sildenafil administered orally 3 times per day 20 mg for the first 2 weeks, followed by 3 times 60 mg for 10 weeks
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo tablets 3 times per day 20 mg foor de first 2 weeks, followed by 3 times 60 mg for 10 weeks
Primary Outcome Measure Information:
Title
Mean Pulmonary Artery Pressure Measured by Right Heart Catheterization
Description
change of mean pulmonary artery pressure between baseline and 12 weeks measured by heart catheterisation
Time Frame
baseline and 12 weeks
Secondary Outcome Measure Information:
Title
VO2max
Description
difference in change of VO2 max between baseline and 12 weeks between Sildenafil and placebo group
Time Frame
baseline and 12 weeks
Title
Cardiac Output Measured Invasively by Right Heart Catheterization
Description
difference in change of cardiac output between baseline and 12 weeks between Sildenafil and Placebo group
Time Frame
baseline and 12 weeks
Title
Wedge Pressure Measured Invasively by Right Heart Catheterization
Description
Difference in change of wedge pressure between baseline and 12 weeks between Sildenafil group and Placebo group
Time Frame
baseline and 12 weeks
Other Pre-specified Outcome Measures:
Title
Echocardiographic Parameters of Diastolic LV Dysfunction
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
E S Hoendermis, MD PhD
Organizational Affiliation
University Medical Center Groningen
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Medical Center Groningen
City
Groningen
ZIP/Postal Code
9700 RB
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
27873388
Citation
Liu LC, Hummel YM, van der Meer P, Berger RM, Damman K, van Veldhuisen DJ, Voors AA, Hoendermis ES. Effects of sildenafil on cardiac structure and function, cardiopulmonary exercise testing and health-related quality of life measures in heart failure patients with preserved ejection fraction and pulmonary hypertension. Eur J Heart Fail. 2017 Jan;19(1):116-125. doi: 10.1002/ejhf.662. Epub 2016 Nov 21.
Results Reference
derived
PubMed Identifier
26188003
Citation
Hoendermis ES, Liu LC, Hummel YM, van der Meer P, de Boer RA, Berger RM, van Veldhuisen DJ, Voors AA. Effects of sildenafil on invasive haemodynamics and exercise capacity in heart failure patients with preserved ejection fraction and pulmonary hypertension: a randomized controlled trial. Eur Heart J. 2015 Oct 7;36(38):2565-73. doi: 10.1093/eurheartj/ehv336. Epub 2015 Jul 17.
Results Reference
derived

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

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