NCT01301625

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

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
78

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Nov 2011

Typical duration for all trials

Geographic Reach
1 country

6 active sites

Status
terminated

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

Completed
19 days until next milestone

First Posted

Study publicly available on registry

February 23, 2011

Completed
8 months until next milestone

Study Start

First participant enrolled

November 1, 2011

Completed
2.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2014

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2014

Completed
4.1 years until next milestone

Results Posted

Study results publicly available

October 22, 2018

Completed
Last Updated

November 7, 2018

Status Verified

November 1, 2018

Enrollment Period

2.8 years

First QC Date

February 4, 2011

Results QC Date

May 18, 2017

Last Update Submit

November 5, 2018

Conditions

Keywords

MitraClipmitral regurgitation (MR)mitral valve insufficiencypercutaneous mitral valve repaircongestive heart failure

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

Device: MitraClip Implant

Interventions

Percutaneous mitral valve repair using MitraClip implant.

Also known as: MitraClip System, MitraClip Delivery System, Steerable Guide Catheter
MitraClip Implant

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Study Sites (6)

St. Vincent's Hospital Sydney

Darlinghurst, New South Wales, 2010, Australia

Location

Macquarie University Hosptial

North Ryde, New South Wales, 2109, Australia

Location

North Shore Private Hospital

St Leonards, New South Wales, 2065, Australia

Location

The Prince Charles Hospital

Chermside, Queensland, 4032, Australia

Location

Flinders Medical Centre

Bedford Park, South Australia, 5042, Australia

Location

Sir Charles Gairdner Hospital

Nedlands, Western Australia, 6009, Australia

Location

Related Publications (103)

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MeSH Terms

Conditions

Mitral Valve InsufficiencyHeart Failure

Condition Hierarchy (Ancestors)

Heart Valve DiseasesHeart DiseasesCardiovascular Diseases

Results Point of Contact

Title
Jeffrey T. Ellis
Organization
Abbott Vascular

Study Officials

  • David Muller, MD

    St Vincent's Hospital - Sydney, Australia

    PRINCIPAL INVESTIGATOR
  • Jurgen Passage, FRACs

    Sir Charles Gairdner Hospital, Perth, Australia

    PRINCIPAL INVESTIGATOR

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

Locations