NCT03975998

Brief Summary

Rationale: 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: in the study of Enriquez-Sarano et al. for instance, 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 \[1\]. 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 (50% at 10 years follow-up according to Rosenhek et al \[2\]), it has proven to be eventually associated with good perioperative and postoperative outcome when careful follow-up is being carried out \[2\]. Objective: To compare early MV repair versus watchful waiting in asymptomatic patients with severe organic mitral valve regurgitation and preserved left ventricular function. Study design: Multicenter, registry trial. Study population: 250 Asymptomatic patients (18-75 years old) with severe organic MV regurgitation and preserved left ventricular function. The current European Society of Cardiology (ESC) guidelines on Valvular Heart Disease will be applied \[3\]. These guidelines are also used in the Netherlands. Accordingly, patients with an indication for MV surgery will not be included. Intervention: Intervention will be early MV repair compared to a watchful waiting strategy.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
500

participants targeted

Target at P75+ for all trials

Timeline
66mo left

Started Oct 2016

Longer than P75 for all trials

Geographic Reach
1 country

6 active sites

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress64%
Oct 2016Oct 2031

Study Start

First participant enrolled

October 1, 2016

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

November 28, 2016

Completed
2.5 years until next milestone

First Posted

Study publicly available on registry

June 5, 2019

Completed
7.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2026

Expected
5 years until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2031

Last Updated

June 6, 2019

Status Verified

June 1, 2019

Enrollment Period

10 years

First QC Date

November 28, 2016

Last Update Submit

June 5, 2019

Conditions

Keywords

Mitral regurgitationMitral repairWatchful waitingAsymptomatic

Outcome Measures

Primary Outcomes (1)

  • Time to event: cardiovascular mortality, congestive heart failure, hospitalization, class I or class IIa indication for MV surgery

    5 years

Study Arms (1)

Aymptomatic patients with severe mitral regurgitation

Watchful waiting Early Surgery

Procedure: Mitral valve repair

Interventions

Minimally invasive repair of severe organic mitral regurgiation

Aymptomatic patients with severe mitral regurgitation

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Asymptomatic patients with severe organic mitral regurgitation and preserved ejection fraction.

You may qualify if:

  • years.
  • Asymptomatic patients. "Asymptomatic" is defined as absence of subjective limitations of exercise capacity or complaints expressed by the patient and confirmed by the treating cardiologist.
  • Severe organic mitral valve regurgitation. "Severe organic mitral valve regurgitation" is defined as non-ischemic mitral valve regurgitation with an organic cause (intrinsic valve lesion) as determined by echocardiographic core-lab reading based on the criteria for definition of severe MR as issued by the ESC guidelines \[4\]. For practical reasons, referring cardiologists can use an ESC guidelines based index that was validated in the investigator's core-lab (Jansen et al, Practical echocardiographic semi-quantitative scoring system to determine severity of mitral regurgitation. Abstract presentation at ESC EUROECHO Congress 2011 and annual spring congress 2012 Netherlands Society of Cardiology).
  • Preserved left ventricular function, "Preserved left ventricular function" is defined as left ventricular ejection fraction \>60% and left ventricular end-systolic dimension \<45 mm (no indexed value, measured by echocardiography).
  • The likelihood of MV repair should be more than 90% determined by the local heart team with a cardiologist and cardiothoracic surgeon.

You may not qualify if:

  • Pulmonary hypertension (\>50 mmHg at rest).
  • Atrial fibrillation, either on 12-lead ECG or holter-monitoring.
  • 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.
  • Patients with moderate to severe kidney disease (estimated glomerular filtration rate (eGFR) less than 30 mL/min).
  • Flail leaflet together with a left ventricular end systolic diameter (LVESD) ≥40 mm (no indexed value)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (6)

Amsterdam Medical Center (AMC)

Amsterdam, Netherlands

RECRUITING

Amphia Breda

Breda, Netherlands

RECRUITING

Medisch Spectrum Twente (MST)

Enschede, Netherlands

RECRUITING

Leiden University Medical Center (LUMC)

Leiden, Netherlands

ACTIVE NOT RECRUITING

Maastricht UMC

Maastricht, Netherlands

RECRUITING

University Medical Center Utrecht (UMC Utrecht)

Utrecht, 3584 CX, Netherlands

RECRUITING

Related Publications (3)

  • 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.

    PMID: 9323067BACKGROUND
  • 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.

    PMID: 16651470BACKGROUND
  • Vahanian A, Baumgartner H, Bax J, Butchart E, Dion R, Filippatos G, Flachskampf F, Hall R, Iung B, Kasprzak J, Nataf P, Tornos P, Torracca L, Wenink A; Task Force on the Management of Valvular Hearth Disease of the European Society of Cardiology; ESC Committee for Practice Guidelines. Guidelines on the management of valvular heart disease: The Task Force on the Management of Valvular Heart Disease of the European Society of Cardiology. Eur Heart J. 2007 Jan;28(2):230-68. doi: 10.1093/eurheartj/ehl428. Epub 2007 Jan 26. No abstract available.

    PMID: 17259184BACKGROUND

MeSH Terms

Conditions

Mitral Valve Insufficiency

Interventions

Mitral Valve Annuloplasty

Condition Hierarchy (Ancestors)

Heart Valve DiseasesHeart DiseasesCardiovascular Diseases

Intervention Hierarchy (Ancestors)

Cardiac Valve AnnuloplastyCardiac Surgical ProceduresCardiovascular Surgical ProceduresSurgical Procedures, OperativeThoracic Surgical Procedures

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
5 Years
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
MD, PhD

Study Record Dates

First Submitted

November 28, 2016

First Posted

June 5, 2019

Study Start

October 1, 2016

Primary Completion (Estimated)

October 1, 2026

Study Completion (Estimated)

October 1, 2031

Last Updated

June 6, 2019

Record last verified: 2019-06

Data Sharing

IPD Sharing
Will not share

Locations