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The Dutch Asymptomatic Mitral Regurgitation Trial (Dutch AMR)

Primary Purpose

Heart; Disease, Mitral(Valve), Diseases of Mitral Valve, Mitral Valve Insufficiency

Status
Terminated
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Watchful waiting
Early mitral valve repair
Sponsored by
UMC Utrecht
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart; Disease, Mitral(Valve) focused on measuring Mitral Valve Insufficiency, Mitral Valve Regurgitation, Asymptomatic Mitral Valve Regurgitation, Asymptomatic Mitral Valve Insufficiency, Mitral Valve Repair, Watchful Waiting

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Asymptomatic
  • Severe organic mitral valve regurgitation.
  • Preserved left ventricular function (left ventricular ejection fraction >60% and left ventricular end-systolic dimension ≤45 mm)
  • The likelihood of MV repair should be more than 90% determined by the local heart team with a cardiologist and cardiothoracic surgeon

Exclusion Criteria:

  • Pulmonary hypertension (>50 mmHg at rest)
  • Atrial fibrillation
  • Physical inability as determined by the heart team to undergo surgery
  • Other life-threatening morbidity
  • Higher expected surgical risks in advance, according to the dedicated heart team
  • Moderate to severe kidney disease (eGFR less than 30 mL/min)
  • Flail leaflet together with a left ventricular end systolic diameter (LVESD) >40 mm

Sites / Locations

  • Leiden University Medical Center
  • Amsterdam Medisch Centrum
  • Amphia Hospital
  • University Medical Center Utrecht (UMC Utrecht)

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Early mitral valve repair

Watchful waiting

Arm Description

Early mitral valve repair

Watchful waiting

Outcomes

Primary Outcome Measures

Composite endpoint: cardiovascular mortality, congestive heart failure and hospitalization for nonfatal cardiovascular events
The primary outcome is defined as 'time to first event'. It concerns time to first event of the composite endpoint of cardiovascular mortality, congestive heart failure, non-fatal cardiovascular events requiring hospitalization, defined as: stroke/cerebrovascular accident (CVA), atrial fibrillation (permanent or requiring hospitalization) and/or reoperation after elective MV surgery.

Secondary Outcome Measures

Cardiovascular mortality
Secondary outcome measures are the separate components of the composite primary endpoint: cardiovascular mortality, congestive heart failure, hospitalization for nonfatal cardiovascular events (stroke/cerebrovascular accident (CVA), AF (permanent or requiring hospitalization) and reoperation after elective MV surgery).
Congestive heart failure
Secondary outcome measures are the separate components of the composite primary endpoint: cardiovascular mortality, congestive heart failure, hospitalization for nonfatal cardiovascular events (stroke/cerebrovascular accident (CVA), AF (permanent or requiring hospitalization) and reoperation after elective MV surgery).
Hospitalization for nonfatal cardiovascular events
Secondary outcome measures are the separate components of the composite primary endpoint: cardiovascular mortality, congestive heart failure, hospitalization for nonfatal cardiovascular events (stroke/cerebrovascular accident (CVA), AF (permanent or requiring hospitalization) and reoperation after elective MV surgery).
All-cause mortality
Secondary outcome measures the incidence of all-cause mortality at a minimum of 5 years.
Costs and effectiveness
Secondary outcome measures total direct and indirect costs and cost-effectiveness at a minimum of 5 years.
Health-related quality of life
Secondary outcome measures health-related quality of life at a minimum of 5 years.
Echocardiographic parameters
Secondary outcome measures echocardiographic parameters at a minimum of 5 years.
CMR parameters
Secondary outcome measures Cardiovascular Magnetic Resonance imaging (CMR) parameters at a minimum of 5 years.
Paroxysmal atrial fibrillation
Secondary outcome measures the incidence of paroxysmal atrial fibrillation at a minimum of 5 years.
Exercise test parameters
Secondary outcome measures exercise test parameters at a minimum of 5 years.
BNP
Secondary outcome measures brain natriuretic peptide (BNP) plasma levels at a minimum of 5 years.
Myocardial infarction
Secondary outcome measures the incidence of myocardial infarction at a minimum of 5 years.
Pacemaker implantation
Secondary outcome measures the incidence of pacemaker implantation at a minimum of 5 years.
Transient ischemic attack
Secondary outcome measures the incidence of transient ischemic attack (TIA) at a minimum of 5 years.
Pulmonary embolism
Secondary outcome measures the incidence of pulmonary embolism at a minimum of 5 years.

Full Information

First Posted
October 11, 2012
Last Updated
November 22, 2016
Sponsor
UMC Utrecht
Collaborators
Leiden University Medical Center, The Interuniversity Cardiology Institute of the Netherlands, WCN, Dutch Network for Cardiovascular Research
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1. Study Identification

Unique Protocol Identification Number
NCT01708265
Brief Title
The Dutch Asymptomatic Mitral Regurgitation Trial
Acronym
Dutch AMR
Official Title
Dutch AMR; Early Mitral Valve Repair Versus Watchful Waiting in Asymptomatic Patients With Severe Organic Mitral Regurgitation; a Multicenter, Randomised Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
November 2016
Overall Recruitment Status
Terminated
Why Stopped
low inclusion rate
Study Start Date
February 2013 (undefined)
Primary Completion Date
February 2021 (Anticipated)
Study Completion Date
February 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
UMC Utrecht
Collaborators
Leiden University Medical Center, The Interuniversity Cardiology Institute of the Netherlands, WCN, Dutch Network for Cardiovascular Research

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to compare early mitral valve repair versus a watchful waiting strategy in asymptomatic patients with severe organic mitral valve regurgitation and preserved left ventricular function.
Detailed Description
Severe asymptomatic organic mitral valve (MV) regurgitation with preserved left ventricular (LV) function is a challenging clinical entity as data on the recommended treatment strategy for these patients are scarce and conflicting, which is reflected in current guidelines. European guidelines advocate a more conservative strategy i.e. watchful waiting, with yearly echocardiography, whilst American guidelines are more in favour of early surgery to reconstruct the MV, i.e. MV repair (in contrast to MV replacement) in order to prevent future LV dysfunction and complaints. A number of non-randomised trials show a favourable outcome of early surgery and the early surgery strategy has shown to be associated with improved long-term survival, decreased cardiac mortality and decreased morbidity compared with the conservative management [citations 1-3]. On the other hand, non-randomised trials describe also that a conservative strategy (i.e. watchful waiting) can be safely accomplished. If facilitated surgery is performed in this population it has proven to be eventually associated with good perioperative and postoperative outcome in 50% of the patients at 10 years when careful follow-up is being carried out [citation 4]. Non-randomised trials inherently have a number of drawbacks. A randomised trial comparing both strategies and objectivising the best treatment strategy has never been performed. The Dutch AMR (Asymptomatic Mitral Regurgitation) trial is a multicenter, prospective, randomised trial comparing early MV repair versus watchful waiting in asymptomatic patients with severe organic MV regurgitation and preserved LV function [citation 5, 6].

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart; Disease, Mitral(Valve), Diseases of Mitral Valve, Mitral Valve Insufficiency
Keywords
Mitral Valve Insufficiency, Mitral Valve Regurgitation, Asymptomatic Mitral Valve Regurgitation, Asymptomatic Mitral Valve Insufficiency, Mitral Valve Repair, Watchful Waiting

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
12 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Early mitral valve repair
Arm Type
Active Comparator
Arm Description
Early mitral valve repair
Arm Title
Watchful waiting
Arm Type
Active Comparator
Arm Description
Watchful waiting
Intervention Type
Other
Intervention Name(s)
Watchful waiting
Intervention Description
In case of watchful waiting a conservative treatment is performed, based on close monitoring of the patient for clear signs of deterioration that triggers facilitated surgery before left ventricular dysfunction is present.
Intervention Type
Procedure
Intervention Name(s)
Early mitral valve repair
Intervention Description
Patients in the group of early mitral valve repair will be operated by way of routine mitral valve repair procedures in specialized centres.
Primary Outcome Measure Information:
Title
Composite endpoint: cardiovascular mortality, congestive heart failure and hospitalization for nonfatal cardiovascular events
Description
The primary outcome is defined as 'time to first event'. It concerns time to first event of the composite endpoint of cardiovascular mortality, congestive heart failure, non-fatal cardiovascular events requiring hospitalization, defined as: stroke/cerebrovascular accident (CVA), atrial fibrillation (permanent or requiring hospitalization) and/or reoperation after elective MV surgery.
Time Frame
Min. 5 years
Secondary Outcome Measure Information:
Title
Cardiovascular mortality
Description
Secondary outcome measures are the separate components of the composite primary endpoint: cardiovascular mortality, congestive heart failure, hospitalization for nonfatal cardiovascular events (stroke/cerebrovascular accident (CVA), AF (permanent or requiring hospitalization) and reoperation after elective MV surgery).
Time Frame
Min. 5 years
Title
Congestive heart failure
Description
Secondary outcome measures are the separate components of the composite primary endpoint: cardiovascular mortality, congestive heart failure, hospitalization for nonfatal cardiovascular events (stroke/cerebrovascular accident (CVA), AF (permanent or requiring hospitalization) and reoperation after elective MV surgery).
Time Frame
Min. 5 years
Title
Hospitalization for nonfatal cardiovascular events
Description
Secondary outcome measures are the separate components of the composite primary endpoint: cardiovascular mortality, congestive heart failure, hospitalization for nonfatal cardiovascular events (stroke/cerebrovascular accident (CVA), AF (permanent or requiring hospitalization) and reoperation after elective MV surgery).
Time Frame
Min. 5 years
Title
All-cause mortality
Description
Secondary outcome measures the incidence of all-cause mortality at a minimum of 5 years.
Time Frame
Min. 5 years
Title
Costs and effectiveness
Description
Secondary outcome measures total direct and indirect costs and cost-effectiveness at a minimum of 5 years.
Time Frame
Min. 5 years
Title
Health-related quality of life
Description
Secondary outcome measures health-related quality of life at a minimum of 5 years.
Time Frame
Min. 5 years
Title
Echocardiographic parameters
Description
Secondary outcome measures echocardiographic parameters at a minimum of 5 years.
Time Frame
Min. 5 years
Title
CMR parameters
Description
Secondary outcome measures Cardiovascular Magnetic Resonance imaging (CMR) parameters at a minimum of 5 years.
Time Frame
Min. 5 years.
Title
Paroxysmal atrial fibrillation
Description
Secondary outcome measures the incidence of paroxysmal atrial fibrillation at a minimum of 5 years.
Time Frame
Min. 5 years
Title
Exercise test parameters
Description
Secondary outcome measures exercise test parameters at a minimum of 5 years.
Time Frame
Min. 5 years.
Title
BNP
Description
Secondary outcome measures brain natriuretic peptide (BNP) plasma levels at a minimum of 5 years.
Time Frame
Min. 5 years
Title
Myocardial infarction
Description
Secondary outcome measures the incidence of myocardial infarction at a minimum of 5 years.
Time Frame
Min. 5 years
Title
Pacemaker implantation
Description
Secondary outcome measures the incidence of pacemaker implantation at a minimum of 5 years.
Time Frame
Min. 5 years
Title
Transient ischemic attack
Description
Secondary outcome measures the incidence of transient ischemic attack (TIA) at a minimum of 5 years.
Time Frame
Min. 5 years
Title
Pulmonary embolism
Description
Secondary outcome measures the incidence of pulmonary embolism at a minimum of 5 years.
Time Frame
Min. 5 years
Other Pre-specified Outcome Measures:
Title
Surgery complication rate
Description
The complication rate in the mitral valve surgery group (e.g. re-operation for bleeding, pneumonia, residual or recurrent mitral valve regurgitation) will be determined at a minimum of 5 years.
Time Frame
Min. 5 years
Title
Rate for the need of facilitated surgery
Description
Rate for the need of facilitated surgery in the watchful waiting group will be determined at a minimum of 5 years.
Time Frame
Min. 5 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Asymptomatic Severe organic mitral valve regurgitation. Preserved left ventricular function (left ventricular ejection fraction >60% and left ventricular end-systolic dimension ≤45 mm) The likelihood of MV repair should be more than 90% determined by the local heart team with a cardiologist and cardiothoracic surgeon Exclusion Criteria: Pulmonary hypertension (>50 mmHg at rest) Atrial fibrillation Physical inability as determined by the heart team to undergo surgery Other life-threatening morbidity Higher expected surgical risks in advance, according to the dedicated heart team Moderate to severe kidney disease (eGFR less than 30 mL/min) Flail leaflet together with a left ventricular end systolic diameter (LVESD) >40 mm
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steven AJ Chamuleau, MD, PhD
Organizational Affiliation
University Medical Center Utrecht (UMC Utrecht)
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jolanda Kluin, MD, PhD
Organizational Affiliation
University Medical Center Utrecht (UMC Utrecht)
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Robert JM Klautz, Prof. MD PhD
Organizational Affiliation
Leiden University Medical Center (LUMC Leiden)
Official's Role
Principal Investigator
Facility Information:
Facility Name
Leiden University Medical Center
City
Leiden
State/Province
South Holland
ZIP/Postal Code
2333 ZA
Country
Netherlands
Facility Name
Amsterdam Medisch Centrum
City
Amsterdam
Country
Netherlands
Facility Name
Amphia Hospital
City
Breda
Country
Netherlands
Facility Name
University Medical Center Utrecht (UMC Utrecht)
City
Utrecht
ZIP/Postal Code
3584 CX
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
9323067
Citation
Ling LH, Enriquez-Sarano M, Seward JB, Orszulak TA, Schaff HV, Bailey KR, Tajik AJ, Frye RL. Early surgery in patients with mitral regurgitation due to flail leaflets: a long-term outcome study. Circulation. 1997 Sep 16;96(6):1819-25. doi: 10.1161/01.cir.96.6.1819.
Results Reference
background
PubMed Identifier
15745978
Citation
Enriquez-Sarano M, Avierinos JF, Messika-Zeitoun D, Detaint D, Capps M, Nkomo V, Scott C, Schaff HV, Tajik AJ. Quantitative determinants of the outcome of asymptomatic mitral regurgitation. N Engl J Med. 2005 Mar 3;352(9):875-83. doi: 10.1056/NEJMoa041451.
Results Reference
background
PubMed Identifier
19632855
Citation
Chenot F, Montant P, Vancraeynest D, Pasquet A, Gerber B, Noirhomme PH, El Khoury G, Vanoverschelde JL. Long-term clinical outcome of mitral valve repair in asymptomatic severe mitral regurgitation. Eur J Cardiothorac Surg. 2009 Sep;36(3):539-45. doi: 10.1016/j.ejcts.2009.02.063. Epub 2009 Jul 25.
Results Reference
background
PubMed Identifier
16651470
Citation
Rosenhek R, Rader F, Klaar U, Gabriel H, Krejc M, Kalbeck D, Schemper M, Maurer G, Baumgartner H. Outcome of watchful waiting in asymptomatic severe mitral regurgitation. Circulation. 2006 May 9;113(18):2238-44. doi: 10.1161/CIRCULATIONAHA.105.599175. Epub 2006 May 1.
Results Reference
background
PubMed Identifier
22354529
Citation
Tietge WJ, de Heer LM, van Hessen MW, Jansen R, Bots ML, van Gilst W, Schalij M, Klautz RJ, Van den Brink RB, Van Herwerden LA, Doevendans PA, Chamuleau SA, Kluin J. Early mitral valve repair versus watchful waiting in patients with severe asymptomatic organic mitral regurgitation; rationale and design of the Dutch AMR trial, a multicenter, randomised trial. Neth Heart J. 2012 Mar;20(3):94-101. doi: 10.1007/s12471-012-0249-y.
Results Reference
background
PubMed Identifier
25301470
Citation
Jansen R, Kluin J, Chamuleau SA. Research versus clinical practice in asymptomatic patients with severe organic mitral regurgitation and preserved LV function. J Am Coll Cardiol. 2014 Oct 14;64(15):1639-40. doi: 10.1016/j.jacc.2014.07.964. No abstract available.
Results Reference
background
Links:
URL
http://dutchamr.nl/
Description
Dutch AMR study homepage

Learn more about this trial

The Dutch Asymptomatic Mitral Regurgitation Trial

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