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

Primary Purpose

Mitral Valve Prolapse

Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Mitral repair with leaflet preservation
Mitral repair with leaflet resection
Sponsored by
Unity Health Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Mitral Valve Prolapse

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Memorial University
  • Hamilton General Hospital
  • London Health Sciences Centre
  • University of Ottawa Heart InstituteRecruiting
  • St Michael's HospitalRecruiting
  • McGill University Health CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Mitral repair with leaflet preservation

Mitral repair with leaflet resection

Arm Description

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

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

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

Mitral valve area
Age/Sex predicted metabolic equivalent score
Mitral leaflet coaptation height
6-minute walk test
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

Full Information

First Posted
July 30, 2015
Last Updated
December 5, 2018
Sponsor
Unity Health Toronto
Collaborators
Ottawa Heart Institute Research Corporation, London Health Sciences Centre
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1. Study Identification

Unique Protocol Identification Number
NCT02552771
Brief Title
The Canadian Mitral Research Alliance (CAMRA) Trial CardioLink-2
Acronym
CAMRA
Official 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
Study Type
Interventional

2. Study Status

Record Verification Date
December 2018
Overall Recruitment Status
Unknown status
Study Start Date
January 2016 (undefined)
Primary Completion Date
January 2019 (Anticipated)
Study Completion Date
January 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Unity Health Toronto
Collaborators
Ottawa Heart Institute Research Corporation, London Health Sciences Centre

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mitral Valve Prolapse

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Mitral repair with leaflet preservation
Arm Type
Active Comparator
Arm Description
Placing man-made fibers (sutures) to more securely connect the mitral leaflets to the papillary muscles (muscles located in the ventricle).
Arm Title
Mitral repair with leaflet resection
Arm Type
Active Comparator
Arm Description
Removal of one or both of the mitral leaflets that flop or bulge back.
Intervention Type
Procedure
Intervention Name(s)
Mitral repair with leaflet preservation
Intervention Description
Placing man-made fibers (sutures) to more securely connect the mitral leaflets to the papillary muscles (muscles located in the ventricle).
Intervention Type
Procedure
Intervention Name(s)
Mitral repair with leaflet resection
Intervention Description
Removing one or both of the mitral leaflets that flop or bulge back.
Primary Outcome Measure Information:
Title
Mean mitral valve gradient at peak exercise 12-months following repair
Time Frame
12 months following repair
Secondary Outcome Measure Information:
Title
Mitral valve area
Time Frame
12 months following repair
Title
Age/Sex predicted metabolic equivalent score
Time Frame
12 months following repair
Title
Mitral leaflet coaptation height
Time Frame
12 months following repair
Title
6-minute walk test
Time Frame
12 months following repair
Title
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
Time Frame
12 months following repair

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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). Planned mitral valve repair amenable to either a leaflet resection or leaflet preservation surgical repair strategy Exclusion Criteria: Patients with anterior leaflet or commissural prolapse Patients with endocarditis or rheumatic mitral valve disease Patients with mitral annular calcification extending beyond the circumference of one leaflet scallop Patients with significant LV dysfunction defined as a LVEF <40% Patients undergoing concomitant aortic valve surgery Patients unable to undergo bicycle ergometry
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Subodh Verma, MD
Phone
416-864-5997
Email
vermasu@smh.ca
First Name & Middle Initial & Last Name or Official Title & Degree
David Mazer, MD
Phone
416-864-5825
Email
mazerd@smh.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vincent Chan, MD
Organizational Affiliation
Ottawa Heart Institute Research Corporation
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Subodh Verma, MD
Organizational Affiliation
Unity Health Toronto
Official's Role
Principal Investigator
Facility Information:
Facility Name
Memorial University
City
St. John's
State/Province
Newfoundland and Labrador
Country
Canada
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Corey Adams, MD
Phone
709-777-2296
First Name & Middle Initial & Last Name & Degree
Corey Adams, MD
Facility Name
Hamilton General Hospital
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8L 2X2
Country
Canada
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Victor Fan Chu, MD
Phone
1 905 523-0440
Email
chu@HHSC.CA
First Name & Middle Initial & Last Name & Degree
Richard Whitlock, MD
Email
Richard.Whitlock@phri.ca
First Name & Middle Initial & Last Name & Degree
Victor Fan Chu, MD
Facility Name
London Health Sciences Centre
City
London
State/Province
Ontario
ZIP/Postal Code
N6A 5W9
Country
Canada
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Michael Chu, MD
Phone
(519) 663-3593
Email
Michael.Chu@lhsc.on.ca
First Name & Middle Initial & Last Name & Degree
Stephanie Fox
Phone
519-685-8500
Ext
35031
Email
Stephanie.Fox@lhsc.on.ca
First Name & Middle Initial & Last Name & Degree
Michael Chu, MD
Facility Name
University of Ottawa Heart Institute
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1Y 4W7
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Vincent Chan, MD
Phone
613-798-5555
Ext
14253
Email
VChan@ottawaheart.ca
First Name & Middle Initial & Last Name & Degree
Jacqueline Fortier, Msc
Phone
613-798-5555
Ext
18329
Email
JFortier@ottawaheart.ca
First Name & Middle Initial & Last Name & Degree
Vincent Chan, MD
Facility Name
St Michael's Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5B1W8
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Subodh Verma, MD
Phone
(416) 864-5997
Email
vermasu@smh.ca
First Name & Middle Initial & Last Name & Degree
Sanjay Yagnik
Phone
416-864-6060
Ext
6690
Email
YagnikS@smh.ca
First Name & Middle Initial & Last Name & Degree
Subodh Verma, MD
Facility Name
McGill University Health Center
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H4A 3J1
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Benoit de Varennes, MD
Phone
514-934-1934
Ext
34980
Email
benoit.devarennes@muhc.mcgill.ca
First Name & Middle Initial & Last Name & Degree
Carole Albert
Phone
514-934-1934
Ext
35277
Email
carole.albert@muhc.mcgill.ca
First Name & Middle Initial & Last Name & Degree
Benoit de Varennes, MD

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

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