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Safety and Efficacy Study of the PTMA Device to Reduce Mitral Valve Regurgitation in Patients With Heart Failure (PTOLEMY2Canada)

Primary Purpose

Mitral Regurgitation, Heart Failure

Status
Suspended
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Percutaneous transvenous mitral annuloplasty
Sponsored by
Viacor
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Mitral Regurgitation focused on measuring mitral valve, heart failure, mitral regurgitation, annuloplasty, coronary sinus

Eligibility Criteria

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

Inclusion Criteria:

  • Patient has moderate functional MR: regurgitant orifice area >/= 0.20cm2 or regurgitant volume >/= 30 mL/beat or regurgitant fraction >/= 30%
  • Symptomatic heart failure NYHA Class II to IV
  • LV dysfunction (25% < LVEF < 50% by echocardiography) OR dilated mitral annulus > 30mm

Exclusion Criteria:

  • MR of organic origin
  • Severe mitral leaflet tethering
  • History of MI or PCI within 60 days of study procedure
  • Inability to walk a minimum of 100 meters in 6 minutes
  • Significant left main stenosis or proximal circumflex stent
  • Indication of non-patent CSO or discontinuous CS-GCV-AIV
  • Bi-ventricular with leads in CS or other devices impeding device placement
  • Severe aortic valvular disease
  • Chronic corticosteroid use other than < 20mg prednisone for arthritis
  • Significant co-morbidities

Sites / Locations

  • University of Ottawa Heart Institute
  • Royal Victoria Hospital, McGill University Medical Center
  • Laval Hospital, Quebec Heart-Lung Institute

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

PTMA implanted

Arm Description

Enrolled patients receiving a PTMA implant

Outcomes

Primary Outcome Measures

Reduction of mitral regurgitation
Freedom from major adverse cardiac events (death, MI, emergent cardiac surgery, and stroke).

Secondary Outcome Measures

Improvement of 6 minute walk distance
Improvement in Quality of Life Score
Reduction of mitral regurgitation
Freedom from procedure-related or device-related major adverse events

Full Information

First Posted
December 26, 2008
Last Updated
February 10, 2011
Sponsor
Viacor
Collaborators
Duke University, Medifacts International Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT00815386
Brief Title
Safety and Efficacy Study of the PTMA Device to Reduce Mitral Valve Regurgitation in Patients With Heart Failure
Acronym
PTOLEMY2Canada
Official Title
Safety and Efficacy of Percutaneous Transvenous Mitral Annuloplasty System to Reduce Mitral Valve Regurgitation in Patients With Heart Failure
Study Type
Interventional

2. Study Status

Record Verification Date
February 2011
Overall Recruitment Status
Suspended
Why Stopped
Company ended operations in January 2011
Study Start Date
February 2009 (undefined)
Primary Completion Date
December 2010 (Actual)
Study Completion Date
December 2015 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Viacor
Collaborators
Duke University, Medifacts International Corporation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Improvement in heart failure with moderate to severe mitral regurgitation using a percutaneously delivered implantable device residing in the coronary sinus
Detailed Description
Device under Test: The Viacor® Percutaneous Transvenous Mitral Annuloplasty (PTMA) system comprises a sterile implantable cardiac device and associated custom accessories to assist implantation. The PTMA system is intended to treat functional mitral regurgitation (MR) in a heart failure patient by a less invasive method than surgical annuloplasty with greater relief of symptoms than medical management alone. Study Objective: Functional mitral regurgitation is associated with an adverse prognosis in the heart failure patient. The objective of this study is to evaluate whether PTMA is effective in reducing mitral regurgitation in heart failure patients and whether this reduction is associated with a moderation in the adverse progression of heart failure symptoms. Hypothesis under Test: Reduction of the severity of functional mitral regurgitation from baseline, as defined by a composite improvement of quantitative echocardiographic metrics, can be achieved safely with the PTMA device and will be associated with a measurable moderation of adverse progression of heart failure symptoms and a moderation of the deterioration of exercise capacity.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mitral Regurgitation, Heart Failure
Keywords
mitral valve, heart failure, mitral regurgitation, annuloplasty, coronary sinus

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
PTMA implanted
Arm Type
Experimental
Arm Description
Enrolled patients receiving a PTMA implant
Intervention Type
Device
Intervention Name(s)
Percutaneous transvenous mitral annuloplasty
Other Intervention Name(s)
mitral annuloplasty, sinoplasty
Intervention Description
Catheterization procedure with anesthesia requiring subclavicular puncture, catheterization of the right atrium and coronary sinus vein, placement and optimization of the PTMA device with access hub remaining subcutaneous at the clavicle.
Primary Outcome Measure Information:
Title
Reduction of mitral regurgitation
Time Frame
6 months
Title
Freedom from major adverse cardiac events (death, MI, emergent cardiac surgery, and stroke).
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Improvement of 6 minute walk distance
Time Frame
6 months
Title
Improvement in Quality of Life Score
Time Frame
6 months
Title
Reduction of mitral regurgitation
Time Frame
6 months
Title
Freedom from procedure-related or device-related major adverse events
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient has moderate functional MR: regurgitant orifice area >/= 0.20cm2 or regurgitant volume >/= 30 mL/beat or regurgitant fraction >/= 30% Symptomatic heart failure NYHA Class II to IV LV dysfunction (25% < LVEF < 50% by echocardiography) OR dilated mitral annulus > 30mm Exclusion Criteria: MR of organic origin Severe mitral leaflet tethering History of MI or PCI within 60 days of study procedure Inability to walk a minimum of 100 meters in 6 minutes Significant left main stenosis or proximal circumflex stent Indication of non-patent CSO or discontinuous CS-GCV-AIV Bi-ventricular with leads in CS or other devices impeding device placement Severe aortic valvular disease Chronic corticosteroid use other than < 20mg prednisone for arthritis Significant co-morbidities
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Luc Bilodeau, MD
Organizational Affiliation
Montreal Heart Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Ottawa Heart Institute
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1Y 4W7
Country
Canada
Facility Name
Royal Victoria Hospital, McGill University Medical Center
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H3A1A1
Country
Canada
Facility Name
Laval Hospital, Quebec Heart-Lung Institute
City
Quebec City
State/Province
Quebec
ZIP/Postal Code
G1V4G5
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
17525965
Citation
Dubreuil O, Basmadjian A, Ducharme A, Thibault B, Crepeau J, Lam JY, Bilodeau L. Percutaneous mitral valve annuloplasty for ischemic mitral regurgitation: first in man experience with a temporary implant. Catheter Cardiovasc Interv. 2007 Jun 1;69(7):1053-61. doi: 10.1002/ccd.21186.
Results Reference
background
PubMed Identifier
18592924
Citation
Fukuda S, Gillinov AM, Liddicoat JR, Saracino G, Hayase M, Cohn WE, Schneider CW, Shiota T. Maintenance of geometric alterations associated with percutaneous mitral valve repair: real-time three-dimensional echocardiographic assessment in an ovine model. J Heart Valve Dis. 2008 May;17(3):276-82.
Results Reference
background
PubMed Identifier
17400117
Citation
Daimon M, Gillinov AM, Liddicoat JR, Saracino G, Fukuda S, Koyama Y, Hayase M, Cohn WE, Ellis SG, Thomas JD, Shiota T. Dynamic change in mitral annular area and motion during percutaneous mitral annuloplasty for ischemic mitral regurgitation: preliminary animal study with real-time 3-dimensional echocardiography. J Am Soc Echocardiogr. 2007 Apr;20(4):381-8. doi: 10.1016/j.echo.2006.08.029.
Results Reference
background
PubMed Identifier
17645049
Citation
Noble S, Bilodeau L. [Percutaneous therapies for aortic and mitral valvular disease]. Rev Med Suisse. 2007 May 30;3(113):1360-1, 1363-4, 1366-7. French.
Results Reference
background
PubMed Identifier
15851597
Citation
Daimon M, Shiota T, Gillinov AM, Hayase M, Ruel M, Cohn WE, Blacker SJ, Liddicoat JR. Percutaneous mitral valve repair for chronic ischemic mitral regurgitation: a real-time three-dimensional echocardiographic study in an ovine model. Circulation. 2005 May 3;111(17):2183-9. doi: 10.1161/01.CIR.0000163547.03188.AC. Epub 2005 Apr 25.
Results Reference
background
PubMed Identifier
14571496
Citation
Liddicoat JR, Mac Neill BD, Gillinov AM, Cohn WE, Chin CH, Prado AD, Pandian NG, Oesterle SN. Percutaneous mitral valve repair: a feasibility study in an ovine model of acute ischemic mitral regurgitation. Catheter Cardiovasc Interv. 2003 Nov;60(3):410-6. doi: 10.1002/ccd.10662.
Results Reference
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Safety and Efficacy Study of the PTMA Device to Reduce Mitral Valve Regurgitation in Patients With Heart Failure

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