Mitral Valve Prolapse Clinical Trial
— CAMRAOfficial title:
A Randomized Trial of Mitral Valve Repair With Leaflet Resection Versus Leaflet Preservation on Functional Mitral Stenosis: The Canadian Mitral Research Alliance (CAMRA-1) Trial
NCT number | NCT02552771 |
Other study ID # | 15-162 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | January 2016 |
Est. completion date | January 2020 |
Multicentre, double-armed, randomized controlled trial designed to compare mitral valve leaflet resection versus leaflet preservation with regards to the development of functional mitral stenosis following surgical repair of mitral valve prolapse. Patients will be randomized (1:1) to receive: (1) mitral valve repair with a leaflet resection or (2) mitral valve repair with leaflet preservation (using polytetrafluoroethylene neochordae), followed by echocardiographic and clinical assessment at 12-months following surgery.
Status | Recruiting |
Enrollment | 104 |
Est. completion date | January 2020 |
Est. primary completion date | January 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: 1. Patients with mitral regurgitation and mitral valve prolapse who are scheduled for elective mitral valve repair by an experienced mitral valve repair surgeon (>15 degenerative mitral valve repairs per year, with a repair rate>90%, and able to perform mitral repair with either a leaflet resection or leaflet preservation strategy). 2. Planned mitral valve repair amenable to either a leaflet resection or leaflet preservation surgical repair strategy Exclusion Criteria: 1. Patients with anterior leaflet or commissural prolapse 2. Patients with endocarditis or rheumatic mitral valve disease 3. Patients with mitral annular calcification extending beyond the circumference of one leaflet scallop 4. Patients with significant LV dysfunction defined as a LVEF <40% 5. Patients undergoing concomitant aortic valve surgery 6. Patients unable to undergo bicycle ergometry |
Country | Name | City | State |
---|---|---|---|
Canada | Hamilton General Hospital | Hamilton | Ontario |
Canada | London Health Sciences Centre | London | Ontario |
Canada | McGill University Health Center | Montreal | Quebec |
Canada | University of Ottawa Heart Institute | Ottawa | Ontario |
Canada | Memorial University | St. John's | Newfoundland and Labrador |
Canada | St Michael's Hospital | Toronto | Ontario |
Lead Sponsor | Collaborator |
---|---|
St. Michael's Hospital, Toronto | London Health Sciences Centre, Ottawa Heart Institute Research Corporation |
Canada,
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* Note: There are 28 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Mean mitral valve gradient at peak exercise 12-months following repair | 12 months following repair | ||
Secondary | Mitral valve area | 12 months following repair | ||
Secondary | Age/Sex predicted metabolic equivalent score | 12 months following repair | ||
Secondary | Mitral leaflet coaptation height | 12 months following repair | ||
Secondary | 6-minute walk test | 12 months following repair | ||
Secondary | Composite MACE (major adverse cardiovascular event) end-point of recurrent MR =2+, death, or hospital re-admission for congestive heart failure within 12-months of surgery | 12 months following repair |
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