Study Stopped
As recruitment rate was lower than anticipated
MitraClip System in Australia and New Zealand
MitraClipANZ
A Prospective Single Arm Clinical Trial Evaluating the MitraClip System in Australia and New Zealand
1 other identifier
observational
78
1 country
6
Brief Summary
The primary objective of the MitraClip System Australia and New Zealand (ANZ) Clinical Trial is to gather real-world clinical and health-economic outcome data to support the long-term safety, efficacy and economic value of the MitraClip System in the continuum of therapies for treating MR. Specifically, the following clinical and economic data will be collected: New York Heart Association (NYHA) Functional Class, Six-Minute Walk Test (6MWT) distance, quality of life (QOL) information, echocardiographic measures of left ventricular size and function, and data associated with the index hospitalization, rehospitalizations, concomitant medications and discharge facility to support the MitraClip System economic analysis.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Nov 2011
Typical duration for all trials
6 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 4, 2011
CompletedFirst Posted
Study publicly available on registry
February 23, 2011
CompletedStudy Start
First participant enrolled
November 1, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2014
CompletedResults Posted
Study results publicly available
October 22, 2018
CompletedNovember 7, 2018
November 1, 2018
2.8 years
February 4, 2011
May 18, 2017
November 5, 2018
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Percentage of Participants Experiencing Death (Kaplan-Meier Analysis)
Clinical Endpoint. * Cardiac death is defined as any death in which a cardiac cause cannot be excluded. (This includes but is not limited to acute myocardial infarction, cardiac perforation/pericardial tamponade, arrhythmia or conduction abnormality,cerebrovascular accident within 30 days of the procedure or cerebrovascular accident suspected of being related to the procedure, death due to complication of the procedure, including bleeding, vascular repair, transfusion reaction, or bypass surgery.) * Non-cardiac death is defined as a death not due to cardiac causes (as defined above).
Baseline
Percentage of Participants Experiencing Death (Kaplan-Meier Analysis)
Clinical Endpoint. * Cardiac death is defined as any death in which a cardiac cause cannot be excluded. (This includes but is not limited to acute myocardial infarction, cardiac perforation/pericardial tamponade, arrhythmia or conduction abnormality,cerebrovascular accident within 30 days of the procedure or cerebrovascular accident suspected of being related to the procedure, death due to complication of the procedure, including bleeding, vascular repair, transfusion reaction, or bypass surgery.) * Non-cardiac death is defined as a death not due to cardiac causes (as defined above).
30 days
Percentage of Participants Experiencing Death (Kaplan-Meier Analysis)
Clinical Endpoint. * Cardiac death is defined as any death in which a cardiac cause cannot be excluded. (This includes but is not limited to acute myocardial infarction, cardiac perforation/pericardial tamponade, arrhythmia or conduction abnormality,cerebrovascular accident within 30 days of the procedure or cerebrovascular accident suspected of being related to the procedure, death due to complication of the procedure, including bleeding, vascular repair, transfusion reaction, or bypass surgery.) * Non-cardiac death is defined as a death not due to cardiac causes (as defined above).
6 months
Percentage of Participants Experiencing Death (Kaplan-Meier Analysis)
Clinical Endpoint. * Cardiac death is defined as any death in which a cardiac cause cannot be excluded. (This includes but is not limited to acute myocardial infarction, cardiac perforation/pericardial tamponade, arrhythmia or conduction abnormality,cerebrovascular accident within 30 days of the procedure or cerebrovascular accident suspected of being related to the procedure, death due to complication of the procedure, including bleeding, vascular repair, transfusion reaction, or bypass surgery.) * Non-cardiac death is defined as a death not due to cardiac causes (as defined above).
12 months
Secondary Outcomes (63)
Number of Participants With 0, 1, 2, and 3 MitraClip Devices Implanted
Day 0 (On the day of procedure)
Number of Participants With Acute Procedural Success Rate
At day 0 (on the day of index procedure)
Procedure Time
At day 0 (on the day of index procedure)
Device Time
At day 0 (on the day of index procedure)
Fluoroscopy Duration
At day 0 (on the day of index procedure)
- +58 more secondary outcomes
Study Arms (1)
MitraClip Implant
Eligible patients undergoing a MitraClip procedure in Australia and New Zealand
Interventions
Percutaneous mitral valve repair using MitraClip implant.
Eligibility Criteria
Consecutive patients eligible to receive the MitraClip implant at the designated investigational sites in Australia and New Zealand.
You may qualify if:
- Age 18 years or older.
- MR ≥ 3+ .
- Transseptal catheterization and femoral vein access feasible.
- Placement of the MitraClip device on mitral leaflets feasible.
- Mitral valve orifice area ≥ 4.0 cm2.
- Written informed consent obtained.
- The patient agrees to return for follow-up visits.
You may not qualify if:
- Need for emergency surgery, other cardiac surgery.
- Coronary artery disease (CAD), atrial fibrillation (AF), other valve disease.
- Prior mitral valve repair surgery, mechanical prosthetic valve, or ventricular assist device (VAD).
- Active endocarditis or rheumatic heart disease; leaflets degenerated from endocarditis or rheumatic disease.
- Transesophageal echocardiography (TEE) contraindicated.
- Known hypersensitivity or contraindication to trial or procedure medications which cannot be managed medically.
- Currently participating in investigational drug trial or another device trial that has not yet completed the primary endpoint or that interferes with the MitraClip System ANZ Clinical Trial.
- Pregnant or planning pregnancy within next 12 months.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Abbott Medical Deviceslead
- Abbottcollaborator
Study Sites (6)
St. Vincent's Hospital Sydney
Darlinghurst, New South Wales, 2010, Australia
Macquarie University Hosptial
North Ryde, New South Wales, 2109, Australia
North Shore Private Hospital
St Leonards, New South Wales, 2065, Australia
The Prince Charles Hospital
Chermside, Queensland, 4032, Australia
Flinders Medical Centre
Bedford Park, South Australia, 5042, Australia
Sir Charles Gairdner Hospital
Nedlands, Western Australia, 6009, Australia
Related Publications (103)
Mauri L, Garg P, Massaro JM, Foster E, Glower D, Mehoudar P, Powell F, Komtebedde J, McDermott E, Feldman T. The EVEREST II Trial: design and rationale for a randomized study of the evalve mitraclip system compared with mitral valve surgery for mitral regurgitation. Am Heart J. 2010 Jul;160(1):23-9. doi: 10.1016/j.ahj.2010.04.009.
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PMID: 22222076BACKGROUNDTamburino C, Ussia GP, Maisano F, Capodanno D, La Canna G, Scandura S, Colombo A, Giacomini A, Michev I, Mangiafico S, Cammalleri V, Barbanti M, Alfieri O. Percutaneous mitral valve repair with the MitraClip system: acute results from a real world setting. Eur Heart J. 2010 Jun;31(11):1382-9. doi: 10.1093/eurheartj/ehq051. Epub 2010 Mar 18.
PMID: 20299349BACKGROUNDUssia GP, Barbanti M, Tamburino C. Feasibility of percutaneous transcatheter mitral valve repair with the MitraClip system using conscious sedation. Catheter Cardiovasc Interv. 2010 Jun 1;75(7):1137-40. doi: 10.1002/ccd.22415.
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PMID: 20583881BACKGROUNDArgenziano M, Skipper E, Heimansohn D, Letsou GV, Woo YJ, Kron I, Alexander J, Cleveland J, Kong B, Davidson M, Vassiliades T, Krieger K, Sako E, Tibi P, Galloway A, Foster E, Feldman T, Glower D; EVEREST Investigators. Surgical revision after percutaneous mitral repair with the MitraClip device. Ann Thorac Surg. 2010 Jan;89(1):72-80; discussion p 80. doi: 10.1016/j.athoracsur.2009.08.063.
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PMID: 21301624BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Results Point of Contact
- Title
- Jeffrey T. Ellis
- Organization
- Abbott Vascular
Study Officials
- PRINCIPAL INVESTIGATOR
David Muller, MD
St Vincent's Hospital - Sydney, Australia
- PRINCIPAL INVESTIGATOR
Jurgen Passage, FRACs
Sir Charles Gairdner Hospital, Perth, Australia
Publication Agreements
- PI is Sponsor Employee
- No
- Restriction Type
- LTE60
- Restrictive Agreement
- Yes
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 4, 2011
First Posted
February 23, 2011
Study Start
November 1, 2011
Primary Completion
September 1, 2014
Study Completion
September 1, 2014
Last Updated
November 7, 2018
Results First Posted
October 22, 2018
Record last verified: 2018-11