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Mitral Annuloplasty Rings RCT

A Study to Assess the Effects of Two Commonly Used Mitral Valve Annuloplasty Rings in Mitral Valve Repair on Short-term Outcomes.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03290872
Enrollment
50
Registered
2017-09-25
Start date
2017-09-30
Completion date
2019-09-30
Last updated
2017-09-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Degenerative Mitral Valve Disease

Brief summary

Recently published work has suggested that mitral valve annuloplasty ring type may affect the development of post-repair mitral stenosis resulting in adverse intracardiac hemodynamics and poor functional status. However, these results have not been comprehensively determined in a systematic manner on a general mitral valve repair population. As well, an underlying mechanism for these findings is not understood. The investigators hypothesize that mitral valve repair with a complete annuloplasty ring (Carpentier-Edwards Physio II) when compared to repair with a partial annuloplasty ring (Simplici- T) may not necessarily result in elevated mitral gradients consistent with functional mitral stenosis (FMS). Currently no prospective data exists to test the hypothesis that a correctly sized, flexible complete annuloplasty ring has detrimental effects. As 60% of annuloplasty rings used in surgical repair of degenerative mitral valve disease in North America utilizes one of the many forms of complete flexible rings available, this information is urgently required. The investigators will evaluate: 1) the effect on mitral valve hemodynamics, 2) changes to mitral annular, valvular and subvalvular structure and function with 3D echocardiography, and 3) the effect on patient functional capacity at 1 year. If FMS early post repair is a real phenomenon, the investigators hope to better understand the mechanisms through the use of advanced imaging techniques-namely 3D modeling of the mitral valvular apparatus, aortic mitral interactions and LV remodeling.

Interventions

DEVICECarpentier Edwards Physio 2 Complete flexible mitral ring

Mitral valve Annuloplasty Ring repair using a Carpentier Edwards Physio 2 Complete flexible mitral ring

DEVICESimplici T Partial flexible mitral annuloplasty ring

Mitral valve Annuloplasty Ring repair using a Simplici T Partial flexible mitral annuloplasty ring

Sponsors

University Health Network, Toronto
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Mitral regurgitation secondary to degenerative valve disease referred to Prof Tirone David (Co-investigator) will be invited to take part. * The mitral valve anatomy must be anatomy suitable for repair. * The patient must be able to perform treadmill exercise echocardiography. * The patient must be over 18 years of age.

Exclusion criteria

* Any presence of life-limiting disease process, for example advanced malignancy. * Hemodynamically unstable patients in cardiogenic shock * Concomitant aortic valve disease/surgery * Previous mitral valve repair * Impaired left ventricular systolic function as defined by a left ventricular ejection fraction of ≤ 50%. * If the patient lives out of state or cannot attend follow up visits.

Design outcomes

Primary

MeasureTime frameDescription
Mean mitral valve gradient1 yearMean mitral valve gradient measured by transthoracic echocardiogram

Secondary

MeasureTime frameDescription
Left ventricular remodelling1 yearAssessment of left ventricular remodelling obtained from transthoracic echocardiography performed pre-operatively and at 1 year post surgery using 3D LV end-diastolic volume and 3D end-systolic volume measurements and 3D LV ejection fraction
Aortic-mitral coupling1 year3D transesophageal echocardiogram assessment intra-operatively both pre and post bypass assessing the entire mitral valvular and subvalvular apparatus, the left ventricle and the aortic valve to assess aortic-mitral valvular coupling and to determine whether there is a difference observed in aorto-mitral coupling between complete and partial ring repairs
Change in functional capacity1 yearFunctional capacity will be specifically assessed using workload achieved on stress transthoracic echocardiogram studies performed pre surgery and at 1 year post surgery. Measurements acquired will include total exercise time and total workload achieved. Also patients will complete SF-36 questionnaires pre-surgery and at 1 year post surgery for further assessment of change in functional capacity

Contacts

Primary ContactWendy W Tsang, MD
Wendy.Tsang@uhn.ca4163403155
Backup ContactKate H Rankin, MBBS
kate.rankin@uhn.ca4163403155

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026