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The Canadian Mitral Research Alliance (CAMRA) Trial CardioLink-2

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02552771
Acronym
CAMRA
Enrollment
104
Registered
2015-09-17
Start date
2016-01-31
Completion date
2020-01-31
Last updated
2018-12-07

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

Conditions

Mitral Valve Prolapse

Brief summary

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.

Detailed description

Mitral valve repair has emerged as the preferred surgical treatment for mitral valve prolapse (MVP), a condition wherein the mitral valve does not close properly. One common strategy for mitral valve repair is leaflet resection, which involves removing part of one or both of the mitral leaflets that flop or bulge back (prolapse). Another strategy is leaflet preservation, which involves placing man-made fibers (sutures) to more securely connect the mitral leaflets to the papillary muscles (muscles located in the ventricle). While both strategies are routinely used and lead to successful mitral valve repair, there is no clear evidence as to whether one strategy is better than the other in terms of long term outcome. The purpose of this study is to determine if one repair strategy (leaflet resection versus leaflet preservation) leads to better longer term patient outcomes. A total of 88 patients from 6 Canadian centres will be randomly assigned to one of the two strategies. The primary outcome will be functional mitral stenosis (MS) as assessed by 12-month mean mitral valve pressure gradient at peak exercise.

Interventions

PROCEDUREMitral repair with leaflet preservation

Placing man-made fibers (sutures) to more securely connect the mitral leaflets to the papillary muscles (muscles located in the ventricle).

PROCEDUREMitral repair with leaflet resection

Removing one or both of the mitral leaflets that flop or bulge back.

Sponsors

Ottawa Heart Institute Research Corporation
CollaboratorOTHER
London Health Sciences Centre
CollaboratorOTHER
Unity Health Toronto
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Mean mitral valve gradient at peak exercise 12-months following repair12 months following repair

Secondary

MeasureTime frame
Mitral valve area12 months following repair
Age/Sex predicted metabolic equivalent score12 months following repair
Mitral leaflet coaptation height12 months following repair
6-minute walk test12 months following repair
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 surgery12 months following repair

Countries

Canada

Contacts

Primary ContactSubodh Verma, MD
vermasu@smh.ca416-864-5997
Backup ContactDavid Mazer, MD
mazerd@smh.ca416-864-5825

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026