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SIDAMI - Sildenafil and Diastolic Dysfunction After Acute Myocardial Infarction (AMI) (SIDAMI)

Primary Purpose

Heart Failure, Diastolic

Status
Completed
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
Sildenafil
Placebo
Sponsored by
Jacob E Mueller
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

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

Eligibility Criteria

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

Inclusion Criteria:

  • Age >50 years
  • Recent AMI (within 21 days) defined according to ESC/ACC guidelines
  • Doppler echocardiographic signs of elevated filling pressures defined as

    • diastolic E/e' ratio >15, or
    • diastolic E/e' ratio 8-15 and left atrial volume index>32 ml/m2
  • Preserved LV systolic function (EF>45%)
  • Written informed consent

Exclusion Criteria:

  • Ongoing myocardial ischemia
  • Ongoing treatment with nitrates.
  • Poor echocardiographic window
  • Inability to exercise
  • Permanent atrial fibrillation or paced rhythm
  • Planned coronary artery bypass grafting
  • Other noncardiac condition with expected survival less than 6 months
  • Unwilling to participate
  • Known intolerance to sildenafil
  • Non-arteritic anterior ischaemic optic neuropathy

Sites / Locations

  • Rigshospitalet

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

Placebo

sildenafil

Arm Description

placebo 3 x daily

40 mg sildenafil 3 x daily

Outcomes

Primary Outcome Measures

Among 70 patients with a recent AMI randomized to sildenafil 40 mg three times daily compared with placebo to compared Pulmonary wedge pressure, cardiac index and pulmonary artery pressure, at rest and during submaximal exercise.

Secondary Outcome Measures

Among 70 patients with a recent AMI randomized to sildenafil 40 mg three times daily compared with placebo to compared exercise capacity judged by bicycle ergometer testing.
Among 70 patients with a recent AMI randomized to sildenafil 40 mg three times daily compared with placebo to compared changes in NT-pro BNP.

Full Information

First Posted
January 11, 2010
Last Updated
May 23, 2012
Sponsor
Jacob E Mueller
Collaborators
Rigshospitalet, Denmark
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1. Study Identification

Unique Protocol Identification Number
NCT01046838
Brief Title
SIDAMI - Sildenafil and Diastolic Dysfunction After Acute Myocardial Infarction (AMI)
Acronym
SIDAMI
Official Title
SIDAMI - Sildenafil and Diastolic Dysfunction After AMI
Study Type
Interventional

2. Study Status

Record Verification Date
May 2012
Overall Recruitment Status
Completed
Study Start Date
December 2009 (undefined)
Primary Completion Date
March 2012 (Actual)
Study Completion Date
May 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Jacob E Mueller
Collaborators
Rigshospitalet, Denmark

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
In patients with Doppler echocardiographic signs of elevated LV filling pressures despite preserved LV systolic function after AMI treatment with the phosphodiesterase inhibitor sildenafil 40 mg three times daily for 9 weeks will compared with placebo Improve resting LV filling and cardiac hemodynamics. Improve exercise capacity. Improve filling pattern and cardiac hemodynamics during exercise.
Detailed Description
Background: Acute myocardial infarction (AMI) is characterized by regional myocardial damage which may lead to systolic and diastolic dysfunction with a subsequent risk of left ventricular (LV) remodeling, local and systemic neurohormonal activation, vascular dysfunction and development of heart failure. The pathophysiology and prognosis of LV systolic dysfunction after AMI has been the focus of research for several decades. Insights from these studies have led to several therapeutic interventions that improve outcome. In addition to depressed systolic function, clinical or radiographic evidence of heart failure is a consistent and powerful predictor of outcome in patients following AMI. Pulmonary congestion after AMI reflects raised LV filling pressures but is frequently seen after what appears to be only minor myocardial damage. The pathophysiological mechanism for this is incompletely understood but may involve impaired active relaxation of the myocardium and increased LV chamber stiffness, hence, abnormalities in diastolic function. Abnormal LV diastolic function especially when chamber stiffness is increased is characterized by a disproportionate increase in filling pressure during exercise and an inadequate increase of cardiac output. During ventricular diastole the left atrium acts as a conduit between the left ventricle and the pulmonary veins. Thus in case of increased filling pressures left atrial pressure is elevated exposing the pulmonary vascular bed to increased pressures. In accordance pulmonary artery pressure is frequently increased after AMI, even when systolic function is preserved. Several recent studies have demonstrated that Doppler echocardiographic indices suggestive of increased filling pressure and increased pulmonary arterial pressure are associated with excess mortality and morbidity after AMI . The optimal management of this large group of patients is unknown, but in theory lowered preload improved cardiac output especially during exercise and lowering of pulmonary arterial pressure could relive symptoms and improve exercise capacity. Sildenafil is a potent selective phosphodiesterase inhibitor that suppresses degradation of cyclic GMP. In the pulmonary bed this leads to pulmonary vasodilation, in addition sildenafil has been shown to improve endothelium dependent vasodilation thus augmenting abnormal vascular tone . In patients with systolic heart failure sildenafil has been demonstrated to lower pulmonary wedge pressure, improve cardiac index and lower pulmonary arterial pressure without causing systemic hypotension . Thus in theory sildenafil may have beneficial effects in patients at high risk of heart failure. Hypothesis: In patients with Doppler echocardiographic signs of elevated LV filling pressures despite preserved LV systolic function after AMI treatment with the phosphodiesterase inhibitor sildenafil 40 mg three times daily for 9 weeks will compared with placebo Improve resting LV filling and cardiac hemodynamics. Improve exercise capacity. Improve filling pattern and cardiac hemodynamics during exercise. Specific aims Primary aims: Among 70 patients with a recent AMI randomized to treatment with sildenafil 40 mg three times daily compared with placebo for 9 weeks to compare mitral filling pattern, diastolic E/e´ ratio and left atrial volume, pulmonary wedge pressure, cardiac index and pulmonary artery pressure, at rest and during submaximal exercise. Secondary Aims Among 70 patients with a recent AMI randomized to sildenafil 40 mg three times daily compared with placebo to compared exercise capacity judged by bicycle ergometer testing. Among 70 patients with a recent AMI randomized to sildenafil 40 mg three times daily compared with placebo to compared changes in NT-pro BNP. Among 70 patients with a recent AMI randomized to sildenafil 40 mg three times daily compared with placebo to compared changes in diastolic E/e´ ratio during submaximal exercise. Among 70 patients with a recent AMI randomized to sildenafil 40 mg three times daily compared with placebo to compare regional systolic function assessed with tissue tracking. Tertiary aims To assess the correlation between diastolic E/e' and Doppler assessed cardiac index during rest and exercise with pulmonary wedge pressure and cardiac index respectively. To assess the association between exercise capacity and diastolic E/e', LA volume, and nt-proBNP. Among 70 patients with a recent AMI randomized to sildenafil 40 mg three times daily compared with placebo to compare the prevalence of atrial arrhythmias after 9 weeks treatment. Methods Design The study is a prospective single center randomized double blind study. Eligible patients will be randomized to either conventional management and sildenafil for 4 months; or conventional management and placebo treatment. Inclusion criteria Age >50 years Recent AMI (within 21 days) defined according to ESC/ACC guidelines Doppler echocardiographic signs of elevated filling pressures defined as diastolic E/e' ratio >15, or diastolic E/e' ratio 8-15 and left atrial volume index>32 ml/m2 Preserved LV systolic function (EF>45%) Written informed consent Exclusion criteria Ongoing myocardial ischemia Ongoing treatment with nitrates. Poor echocardiographic window Inability to exercise Permanent atrial fibrillation or paced rhythm Planned coronary artery bypass grafting Other noncardiac condition with expected survival less than 6 months Unwilling to participate Known intolerance to sildenafil Study procedures In possibly eligible patients a screening echocardiography is performed during hospitalization at the coronary care unit 2144 or 3141 HS Rigshospitalet, Denmark. If eligible and consent is obtained during hospitalisation an ambulatory exercise Doppler echocardiography with simultaneous invasive recording of pulmonary wedge pressure, pulmonary artery pressure and cardiac index and a 6 min walk test and maximal exercise test is performed 1 week after revascularization. Patients are then randomized in a 1 to 1 fashion to placebo or sildenafil 20 mg three times daily. If tolerated dosage is titrated every 2'nd week in the outpatient clinic to a target dose of 40 mg three times daily. After 9 weeks of treatment exercise echocardiography and 6 min walk test are repeated, in addition conventional maximal ergometer testing is performed. Screening echocardiography 2 dimensional echocardiographic will be obtained from the parasternal and apical windows. Pulsed Doppler measurements of mitral inflow will be obtained with the transducer in the apical four-chamber view, with a 1-2 mm Doppler sample volume placed between the tips of mitral leaflets during diastole. Tissue Doppler imagining of the mitral annulus will be obtained from the apical 4-chamber view with a 1.5-mm sample volume placed at the medial mitral annulus. All Doppler echocardiographic examinations are done with horizontal sweep set to 100 mm/s. At least 3-5 cardiac cycles will be measured. LA volume will be obtained from the apical 4 and 2 chamber views with a zoomed image of the left atrium. Clinically indicted echocardiograms performed in the echolab may be used as screening echocardiograms. Wall motion index will semiquantitatively using a descending scoring as previously validated. Maximal left atrial volume will be measured at end-systole with the use of two orthogonal apical views. From the pulsed wave mitral inflow signal, peak E wave velocity will be measured. From the tissue Doppler assessment of the medial mitral annulus early (E') diastolic velocity will be recorded. Diastolic E/e' ratio will be calculated. Resting echocardiography Doppler echocardiography will be performed on a GE medical Vivid 7 ultrasound machine by a single investigator. Images will be obtained from the parasternal and apical windows. M-mode recordings will be done in the parasternal long-axis view. Pulsed Doppler measurements of mitral inflow will be obtained with the transducer in the apical four-chamber view, with a 1-2 mm Doppler sample volume placed between the tips of mitral leaflets during diastole. Tissue Doppler imagining of the mitral annulus will be obtained from the apical 4-chamber view with a 1.5-mm sample volume placed at the medial and lateral mitral annulus. All Doppler echocardiographic examinations are done with horizontal sweep set to 100 mm/s. At least 3-5 cardiac cycles will be measured. Finally color coded real time tissue Doppler images will be acquired in the apical windows, with the lowest possible depth and smallest angle. End-systolic, end-diastolic volume and ejection fraction will be calculated according to the Simpson modified biplane method. Wall motion index will semiquantitatively be assessed according to the recommendations of the American Society of Echocardiography. Maximal left atrial volume will be measured at end-systole with the use of two orthogonal apical views with zoom of the left atrium. From the pulsed wave mitral inflow signal, peak E wave velocity, peak A wave velocity, and mitral E-wave deceleration time will be measured. From peak tricuspid regurgitant velocity and size of inferior v. cava pulmonary arterial systolic pressure will be estimated. From the tissue Doppler assessment of the medial mitral annulus early (E') diastolic velocity will be recorded. Diastolic E/e' ratio will be calculated. From color coded tissue Doppler images systolic longitudinal fibre shortening will be assessed using tissue tracking. From 2dimensional images speckle tracing will be performed to assess radial and longitudinal LV function. Exercise echocardiography Exercise echocardiography is performed at cardiac intensive care unit 2143. Before exercise a Swan Ganz catheter is introduced with a seldinger technique through the right jugular vein. Simultaneous with resting echocardiography pulmonary artery pressure, left atrial pressure, cardiac index and pulmonary wedge pressure is recorded. Patients are then exercised on a supine bicycle with increasing workload to 100W with increments of 25W every 2'nd min. At 100W echocardiography is repeated with simultaneous assessment of pulmonary artery pressure, left atrial pressure, pulmonary wedge pressure and cardiac index. Neurohormonal analyses Prior to surgery and at each follow-up visit venous blood samples will be drawn for analysis of plasma N-terminal proBNP, and of plasma N-terminal ANP concentrations. In addition plasma will be frozen at each visit for possible later analysis. Six minutes walk test A 6 min. walk test will be performed at baseline 9 weeks. Exercise test A conventional bicycle ergometer test is performed at hospital discharge and after 4 months. Maximal exercise is achieved by increments on 25W every 2'nd min. with continuous ECG recording and assessment of blood pressure every 2'nd min. Feasibility and sample size estimation From a recent study at a tertiary invasive centre including 380 patients with AMI, (Aberdeen AMI study, Hillis et al ESC 2006), it was found that among 219 patients EF was >45%. Among those patients E/e' >15 was found in 41 patients, and in further 48 E/e' 8-15 and left atrial volume index >32 ml/m2 was found. Thus 40% of patients with LVEF>45% would be potentially eligible. Annually 2500 patients are admitted or transferred to RH with AMI. Based on a standard deviation of E/e' of 5 (estimated from potentially eligible patients from the Aberdeen AMI study), an alpha of 0.05 and beta of 0.80 a sample of 70 patients will allow detection of a difference in E/e' of 3.6. Sample size estimation is performed according to Altmann using nomogram.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
70 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
placebo 3 x daily
Arm Title
sildenafil
Arm Type
Active Comparator
Arm Description
40 mg sildenafil 3 x daily
Intervention Type
Drug
Intervention Name(s)
Sildenafil
Other Intervention Name(s)
Revatio, Viagra
Intervention Description
40 mg three times daily for 9 weeks
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
tablet 3 times daily for 9 weeks
Primary Outcome Measure Information:
Title
Among 70 patients with a recent AMI randomized to sildenafil 40 mg three times daily compared with placebo to compared Pulmonary wedge pressure, cardiac index and pulmonary artery pressure, at rest and during submaximal exercise.
Time Frame
9 weeks
Secondary Outcome Measure Information:
Title
Among 70 patients with a recent AMI randomized to sildenafil 40 mg three times daily compared with placebo to compared exercise capacity judged by bicycle ergometer testing.
Time Frame
9 weeks
Title
Among 70 patients with a recent AMI randomized to sildenafil 40 mg three times daily compared with placebo to compared changes in NT-pro BNP.
Time Frame
9 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age >50 years Recent AMI (within 21 days) defined according to ESC/ACC guidelines Doppler echocardiographic signs of elevated filling pressures defined as diastolic E/e' ratio >15, or diastolic E/e' ratio 8-15 and left atrial volume index>32 ml/m2 Preserved LV systolic function (EF>45%) Written informed consent Exclusion Criteria: Ongoing myocardial ischemia Ongoing treatment with nitrates. Poor echocardiographic window Inability to exercise Permanent atrial fibrillation or paced rhythm Planned coronary artery bypass grafting Other noncardiac condition with expected survival less than 6 months Unwilling to participate Known intolerance to sildenafil Non-arteritic anterior ischaemic optic neuropathy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jacob E Møller, MD, Phd, DmSci
Organizational Affiliation
Rigshospitalet, Denmark
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mads J Andersen, MD
Organizational Affiliation
The Heart Center, Cardiology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rigshospitalet
City
Copenhagen
ZIP/Postal Code
2100
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
36356959
Citation
Andersen MJ, Wolsk E, Bakkestrom R, Christensen N, Carter-Storch R, Omar M, Dahl JS, Frederiksen PH, Borlaug B, Gustafsson F, Hassager C, Moller JE. Pressure-flow responses to exercise in aortic stenosis, mitral regurgitation and diastolic dysfunction. Heart. 2022 Nov 10;108(23):1895-1903. doi: 10.1136/heartjnl-2022-321204.
Results Reference
derived
PubMed Identifier
23406672
Citation
Andersen MJ, Ersboll M, Axelsson A, Gustafsson F, Hassager C, Kober L, Borlaug BA, Boesgaard S, Skovgaard LT, Moller JE. Sildenafil and diastolic dysfunction after acute myocardial infarction in patients with preserved ejection fraction: the Sildenafil and Diastolic Dysfunction After Acute Myocardial Infarction (SIDAMI) trial. Circulation. 2013 Mar 19;127(11):1200-8. doi: 10.1161/CIRCULATIONAHA.112.000056. Epub 2013 Feb 13.
Results Reference
derived

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SIDAMI - Sildenafil and Diastolic Dysfunction After Acute Myocardial Infarction (AMI)

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