Myocardial Efficiency of the Left Ventricle in Asymptomatic Patients With Aortic Valve Stenosis - a Prognostic Marker and a Target for Intervention? (MELVAS)
Primary Purpose
Aortic Stenosis
Status
Completed
Phase
Phase 2
Locations
Denmark
Study Type
Interventional
Intervention
Metoprololsuccinate
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Aortic Stenosis focused on measuring Aortic Stenosis, Myocardial efficiency
Eligibility Criteria
Inclusion Criteria:
- Aortic valve area ≤1,2 cm2 and/or transaortic maximal velocity (VmaxAO) of 3,0-5,0 m/s
- Sinus rhythm >60/min after 5 minutes of rest
- LVEF >≥50%
- Male or female
- Age 20-100 years old
- Safe birth control management for women of childbearing potential.
- Negative urine-HCG for women of childbearing potential
- Ability to understand the written patient information and to give informed consent
Exclusion Criteria:
- Systolic BP <100 mmHg after 5 minutes of rest
- Left ventricular posterior wall thickness >17 mm
- Signs or history of major myocardial infarction and/or severe ischemic heart disease
- Severe asthma or chronic obstructive pulmonary disease
- New York Heart Association (NYHA) classification > I due to AS
- NYHA > II due to non-cardiac causes
- 2ᵒ or 3ᵒ atrioventricular block
- Ongoing beta-blocker therapy
- Ongoing verapamil or diltiazem therapy
- Ongoing monoamine oxidase inhibitors therapy (except MAO-B-inhibitors)
- Sick sinus syndrome
- Atrial fibrillation or fluttering
- Lack of stable sinus rhythm
- Pheochromocytoma
- Severe peripheral vascular disease
- Intolerance of Metoprolol succinate or its excipients
- Other disease or treatment making subject unsuitable for study participation
- Intolerance of tracer used for [11C]acetate PET recordings
- Participation in other intervention study
Sites / Locations
- Aarhus University Hospital, Department of Cardiology, Brendstrupgaardsvej 100
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Active
Placebo
Arm Description
Metoprololsuccinate
Placebo
Outcomes
Primary Outcome Measures
LV myocardial efficiency
Secondary Outcome Measures
LV oxygen consumption
LV perfusion
LV myocardial function
LVmass
Aortic valve area
Transaortic valve velocities
6 minute walking distance
N-terminal prohormone of brain natriuretic peptide
Quality of life - estimated by Minnesota living with heart failure questionnaire
LV wall stress
Full Information
NCT ID
NCT02076711
First Posted
February 27, 2014
Last Updated
November 10, 2015
Sponsor
Aarhus University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02076711
Brief Title
Myocardial Efficiency of the Left Ventricle in Asymptomatic Patients With Aortic Valve Stenosis - a Prognostic Marker and a Target for Intervention?
Acronym
MELVAS
Official Title
Myocardial Efficiency of the Left Ventricle in Asymptomatic Patients With Aortic Valve Stenosis - a Prognostic Marker and a Target for Intervention?
Study Type
Interventional
2. Study Status
Record Verification Date
November 2015
Overall Recruitment Status
Completed
Study Start Date
June 2013 (undefined)
Primary Completion Date
September 2015 (Actual)
Study Completion Date
September 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Aarhus University Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Background - Aortic valve stenosis (AS) is the most common heart valve disease among adults in the Western world with a prevalence of 3 % in people older than 75 years of age. AS usually deteriorates over time leading to heart failure, with high mortality if aortic valve replacement (AVR) is not performed. Thus optimal timing of AVR is crucial, but can be challenging. Increasing life expectancy in our society will augment the therapeutic and socio economic impact of AS disease on our health care system. Therefore, new techniques for monitoring asymptomatic AS patients are needed. A potential approach is monitoring of LV myocardial efficiency (mechanical work/oxygen consumption). These measures have been suggested to be involved in the progression of non-valvular heart failure and closely related to prognosis, but never applied in a larger population of patients with AS. At present there are no recognized pharmacological treatments of AS. It is known that beta-blocker treatment in non-valvular systolic heart failure reduce heart rate, improves LV myocardial efficiency and reduces mortality. However, in patients with AS, the effects of beta-blockers are unknown.
Hypotheses - Treatment with the beta-blocker metoprolol succinate in patients with asymptomatic moderate to severe AS has beneficial effects on LV myocardial oxidative metabolism, myocardial efficiency and contractile function.
Objectives - To investigate if beta-blocker treatment in patients with moderate to severe, asymptomatic AS has beneficial effects on LV myocardial efficiency, contractile function and physical performance.
Design - A randomized double blind placebo controlled intervention trial. 40 patients with asymptomatic AS will be randomized to either per oral metoprolol succinate (N = 20) or placebo (N= 20) for 22 weeks.
Primary objective - Changes in myocardial efficiency
Secondary objectives - Myocardial oxygen consumption, Myocardial perfusion at rest, LV myocardial function, LVmass, Aortic valve area and transaortic valve velocities, 6 minute walking distance, N-terminal prohormone of brain natriuretic peptide, Quality of life (estimated by Minnesota living with heart failure questionnaire), LV wall stress
Methods - Patients will undergo echocardiography (resting and exercise), [11C]acetate PET and cardiac magnetic resonance imaging.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Aortic Stenosis
Keywords
Aortic Stenosis, Myocardial efficiency
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
40 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Active
Arm Type
Active Comparator
Arm Description
Metoprololsuccinate
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo
Intervention Type
Drug
Intervention Name(s)
Metoprololsuccinate
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
LV myocardial efficiency
Time Frame
Changes will be evaluated after an expected average of 22 weeks of treatment
Secondary Outcome Measure Information:
Title
LV oxygen consumption
Time Frame
Changes will be evaluated after an expected average of 22 weeks of treatment
Title
LV perfusion
Time Frame
Changes will be evaluated after an expected average of 22 weeks of treatment
Title
LV myocardial function
Time Frame
Changes will be evaluated after an expected average of 22 weeks of treatment
Title
LVmass
Time Frame
Changes will be evaluated after an expected average of 22 weeks of treatment
Title
Aortic valve area
Time Frame
Changes will be evaluated after an expected average of 22 weeks of treatment
Title
Transaortic valve velocities
Time Frame
Changes will be evaluated after an expected average of 22 weeks of treatment
Title
6 minute walking distance
Time Frame
Changes will be evaluated after an expected average of 22 weeks of treatment
Title
N-terminal prohormone of brain natriuretic peptide
Time Frame
Changes will be evaluated after an expected average of 22 weeks of treatment
Title
Quality of life - estimated by Minnesota living with heart failure questionnaire
Time Frame
Changes will be evaluated after an expected average of 22 weeks of treatment
Title
LV wall stress
Time Frame
Changes will be evaluated after an expected average of 22 weeks of treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Aortic valve area ≤1,2 cm2 and/or transaortic maximal velocity (VmaxAO) of 3,0-5,0 m/s
Sinus rhythm >60/min after 5 minutes of rest
LVEF >≥50%
Male or female
Age 20-100 years old
Safe birth control management for women of childbearing potential.
Negative urine-HCG for women of childbearing potential
Ability to understand the written patient information and to give informed consent
Exclusion Criteria:
Systolic BP <100 mmHg after 5 minutes of rest
Left ventricular posterior wall thickness >17 mm
Signs or history of major myocardial infarction and/or severe ischemic heart disease
Severe asthma or chronic obstructive pulmonary disease
New York Heart Association (NYHA) classification > I due to AS
NYHA > II due to non-cardiac causes
2ᵒ or 3ᵒ atrioventricular block
Ongoing beta-blocker therapy
Ongoing verapamil or diltiazem therapy
Ongoing monoamine oxidase inhibitors therapy (except MAO-B-inhibitors)
Sick sinus syndrome
Atrial fibrillation or fluttering
Lack of stable sinus rhythm
Pheochromocytoma
Severe peripheral vascular disease
Intolerance of Metoprolol succinate or its excipients
Other disease or treatment making subject unsuitable for study participation
Intolerance of tracer used for [11C]acetate PET recordings
Participation in other intervention study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Henrik Wiggers, DMSc
Official's Role
Principal Investigator
Facility Information:
Facility Name
Aarhus University Hospital, Department of Cardiology, Brendstrupgaardsvej 100
City
Aarhus N
ZIP/Postal Code
8200
Country
Denmark
12. IPD Sharing Statement
Citations:
PubMed Identifier
28956773
Citation
Hansson NH, Sorensen J, Harms HJ, Kim WY, Nielsen R, Tolbod LP, Frokiaer J, Bouchelouche K, Dodt KK, Sihm I, Poulsen SH, Wiggers H. Metoprolol Reduces Hemodynamic and Metabolic Overload in Asymptomatic Aortic Valve Stenosis Patients: A Randomized Trial. Circ Cardiovasc Imaging. 2017 Oct;10(10):e006557. doi: 10.1161/CIRCIMAGING.117.006557.
Results Reference
derived
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Myocardial Efficiency of the Left Ventricle in Asymptomatic Patients With Aortic Valve Stenosis - a Prognostic Marker and a Target for Intervention?
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