Surgical Septal Myectomy vs Percutaneous Transluminal Alcohol Septal Ablation in Patients With Hypertrophic Obstructive Cardiomyopathy (AMARONE)
Primary Purpose
Hypertrophic Cardiomyopathy
Status
Recruiting
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Alcohol Septal Ablation
Surgical Septal Myectomy
Sponsored by
About this trial
This is an interventional treatment trial for Hypertrophic Cardiomyopathy
Eligibility Criteria
Inclusion Criteria:
- Age between 40-75 years including 40 and 75 years of age
- HOCM eligible for both SSM and ASA by a heart team (multidisciplinary team) and core lab.
- Left ventricle outflow tract (LVOT) obstruction > 30mmHg at rest or during physiological provocation by transthoracic echocardiogram
- Symptomatic (New York Heart Association classification (NYHA) >1 or Canadian Cardiovascular Society (CCS) class >1) and/or syncope due to HOCM
Exclusion Criteria:
- Unable to give informed consent
- A life expectancy of less than 1 year
- Concomitant (structural valve disease, aorta, rhythm, CABG) surgery during the same session
- Not able to perform bicycle ergometry exercise test
Sites / Locations
- St. Antonius HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Alcohol Septal Ablation
Surgical Septal Myectomy
Arm Description
Outcomes
Primary Outcome Measures
Metabolic Equivalent (METs) assessed with a bicycle ergometry exercise test
The primary endpoint is the improvement of the exercise capacity in the form of Metabolic Equivalent (METs) which will be assessed with a bicycle ergometry exercise test (difference in exercise capacity in Metabolic Equivalents) performed before and 1 year after invasive treatment.
Secondary Outcome Measures
Number of participants with all-cause mortality
Number of participants with cardiovascular mortality
Number of participants with transient Ischemic Attack
Number of participants with hospital Readmittance
Number of participants with with occurrence of atrial fibrillation
Number of participants with ventricular arrhythmias
Number of participants with with complete heart block requiring permanent pacemaker implantation
Number of participants with major bleeding
Bleeding rate will be analysed using Bleeding Academic Research Consortium (type 3,4 or 5), TIMI major and VARC major criteria.
Number of participants with re-intervention
One more time need for Alcohol septal ablation or surgical septal myectomy
Blood sample results
Troponin T (in ug/l)
Blood sample results
N-terminal prohormone of brain natriuretic peptide (NT-pro-BNP in pg/ml)
Blood sample results
Creatine-kinase (CK in U/l)
Quality of life evaluation using the The Kansas City Cardiomyopathy Questionnaire (KCCQ)
In the KCCQ, an overall summary score can be derived from the physical function, symptom (frequency and severity), social function and quality of life domains. For each domain, the validity, reproducibility, responsiveness and interpretability have been independently established. Scores are transformed to a range of 0-100, in which higher scores reflect better health status. For brevity, only the performance characteristics of the overall summary score are presented in this discussion.
Cardiac Magnetic Resonance Imaging (CMR) parameters
Interventricular septal thickness (mm), atrial diameter (mm) , left and right ventricular diameter (mm), left ventricle end diastolic volume (ml), left ventricle systolic volume (ml)
Cardiac Magnetic Resonance Imaging (CMR) parameters
Left ventricle end diastolic volume (ml), left ventricle systolic volume (ml)
Transthoracic echocardiogram
Left ventricle ejection fraction (%)
Transthoracic echocardiogram
Left ventricle outflow tract gradient (mmHg)
Transthoracic echocardiogram
Left ventricular internal systolic and diastolic dimension (cm)
Transthoracic echocardiogram
Atrial diameter (ml/m2)
Transthoracic echocardiogram
Valvular function
Transthoracic echocardiogram
Right ventricular systolic pressure (mmHg)
Transthoracic echocardiogram
Interventricular septal thickness (mm)
Full Information
NCT ID
NCT04684290
First Posted
November 16, 2020
Last Updated
September 8, 2021
Sponsor
St. Antonius Hospital
Collaborators
Erasmus Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT04684290
Brief Title
Surgical Septal Myectomy vs Percutaneous Transluminal Alcohol Septal Ablation in Patients With Hypertrophic Obstructive Cardiomyopathy
Acronym
AMARONE
Official Title
Surgical Septal Myectomy Versus Percutaneous Transluminal Alcohol Septal Ablation in Patients With Hypertrophic Obstructive Cardiomyopathy
Study Type
Interventional
2. Study Status
Record Verification Date
September 2021
Overall Recruitment Status
Recruiting
Study Start Date
June 30, 2021 (Actual)
Primary Completion Date
May 1, 2025 (Anticipated)
Study Completion Date
May 1, 2026 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
St. Antonius Hospital
Collaborators
Erasmus Medical Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The aim of this randomized trial is to compare the improvement in exercise capacity among patients with highly symptomatic hypertrophic obstructive cardiomyopathy despite optimal medical treatment who undergo alcohol septal ablation (ASA) or surgical septal myectomy (SSM).
Detailed Description
This is a prospective, multicentre, open label, randomized controlled, non-inferiority trial (RCT) with a 1:1 randomization to alcohol septal ablation or surgical septal myectomy in patients with hypertrophic obstructive cardiomyopathy (HOCM) between 40-75 year of age with symptoms and/or syncope due to HOCM despite medical therapy. A total of 100 patients will be included. All patients will be evaluated with bicycle ergometry exercise test, MRI and 2D-echo before and 1 year after invasive treatment. Follow-up will be at 1,3 and 5 years.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertrophic Cardiomyopathy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Alcohol Septal Ablation
Arm Type
Active Comparator
Arm Title
Surgical Septal Myectomy
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
Alcohol Septal Ablation
Intervention Description
Participants will be treated with alcohol septal ablation.
Intervention Type
Procedure
Intervention Name(s)
Surgical Septal Myectomy
Intervention Description
Participants will be treated with surgical septal myectomy.
Primary Outcome Measure Information:
Title
Metabolic Equivalent (METs) assessed with a bicycle ergometry exercise test
Description
The primary endpoint is the improvement of the exercise capacity in the form of Metabolic Equivalent (METs) which will be assessed with a bicycle ergometry exercise test (difference in exercise capacity in Metabolic Equivalents) performed before and 1 year after invasive treatment.
Time Frame
1 year after the invasive treatment
Secondary Outcome Measure Information:
Title
Number of participants with all-cause mortality
Time Frame
Follow up will be 1,3 and 5 years
Title
Number of participants with cardiovascular mortality
Time Frame
Follow up will be 1,3 and 5 years
Title
Number of participants with transient Ischemic Attack
Time Frame
Follow up will be 1,3 and 5 years
Title
Number of participants with hospital Readmittance
Time Frame
Follow up will be 1,3 and 5 years
Title
Number of participants with with occurrence of atrial fibrillation
Time Frame
Follow up will be 1,3 and 5 years
Title
Number of participants with ventricular arrhythmias
Time Frame
Follow up will be 1,3 and 5 years
Title
Number of participants with with complete heart block requiring permanent pacemaker implantation
Time Frame
Follow up will be 1,3 and 5 years
Title
Number of participants with major bleeding
Description
Bleeding rate will be analysed using Bleeding Academic Research Consortium (type 3,4 or 5), TIMI major and VARC major criteria.
Time Frame
First 30 days
Title
Number of participants with re-intervention
Description
One more time need for Alcohol septal ablation or surgical septal myectomy
Time Frame
Follow up will be 1,3 and 5 years
Title
Blood sample results
Description
Troponin T (in ug/l)
Time Frame
Follow up will be 1,3 and 5 years
Title
Blood sample results
Description
N-terminal prohormone of brain natriuretic peptide (NT-pro-BNP in pg/ml)
Time Frame
Follow up will be 1,3 and 5 years
Title
Blood sample results
Description
Creatine-kinase (CK in U/l)
Time Frame
Follow up will be 1,3 and 5 years
Title
Quality of life evaluation using the The Kansas City Cardiomyopathy Questionnaire (KCCQ)
Description
In the KCCQ, an overall summary score can be derived from the physical function, symptom (frequency and severity), social function and quality of life domains. For each domain, the validity, reproducibility, responsiveness and interpretability have been independently established. Scores are transformed to a range of 0-100, in which higher scores reflect better health status. For brevity, only the performance characteristics of the overall summary score are presented in this discussion.
Time Frame
Follow up will be 1,3 and 5 years
Title
Cardiac Magnetic Resonance Imaging (CMR) parameters
Description
Interventricular septal thickness (mm), atrial diameter (mm) , left and right ventricular diameter (mm), left ventricle end diastolic volume (ml), left ventricle systolic volume (ml)
Time Frame
Follow up will be 1,3 and 5 years
Title
Cardiac Magnetic Resonance Imaging (CMR) parameters
Description
Left ventricle end diastolic volume (ml), left ventricle systolic volume (ml)
Time Frame
Follow up will be 1,3 and 5 years
Title
Transthoracic echocardiogram
Description
Left ventricle ejection fraction (%)
Time Frame
Follow up will be 1,3 and 5 years
Title
Transthoracic echocardiogram
Description
Left ventricle outflow tract gradient (mmHg)
Time Frame
Follow up will be 1,3 and 5 years
Title
Transthoracic echocardiogram
Description
Left ventricular internal systolic and diastolic dimension (cm)
Time Frame
Follow up will be 1,3 and 5 years
Title
Transthoracic echocardiogram
Description
Atrial diameter (ml/m2)
Time Frame
Follow up will be 1,3 and 5 years
Title
Transthoracic echocardiogram
Description
Valvular function
Time Frame
Follow up will be 1,3 and 5 years
Title
Transthoracic echocardiogram
Description
Right ventricular systolic pressure (mmHg)
Time Frame
Follow up will be 1,3 and 5 years
Title
Transthoracic echocardiogram
Description
Interventricular septal thickness (mm)
Time Frame
Follow up will be 1,3 and 5 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age between 40-75 years including 40 and 75 years of age
HOCM eligible for both SSM and ASA by a heart team (multidisciplinary team) and core lab.
Left ventricle outflow tract (LVOT) obstruction > 30mmHg at rest or during physiological provocation by transthoracic echocardiogram
Symptomatic (New York Heart Association classification (NYHA) >1 or Canadian Cardiovascular Society (CCS) class >1) and/or syncope due to HOCM
Exclusion Criteria:
Unable to give informed consent
A life expectancy of less than 1 year
Concomitant (structural valve disease, aorta, rhythm, CABG) surgery during the same session
Not able to perform bicycle ergometry exercise test
Facility Information:
Facility Name
St. Antonius Hospital
City
Nieuwegein
State/Province
Utrecht
ZIP/Postal Code
3435cm
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jurrien ten Berg
Phone
088 320 3000
Email
j.ten.berg@antoniusziekenhuis.nl
12. IPD Sharing Statement
Plan to Share IPD
No
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Surgical Septal Myectomy vs Percutaneous Transluminal Alcohol Septal Ablation in Patients With Hypertrophic Obstructive Cardiomyopathy
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