Medtronic CoreValve REDO Study

NCT01051310 | Completed Results DMC

• 1 other identifier: COR-2007-03
• Study Type: interventional
• Target: 18
• Locations: 2 countries
• Sites: 3

Brief Summary

The proposed investigation is a prospective, multicenter, non-randomized study to evaluate the immediate benefits (at discharge and at 30 days) in terms of performance and safety of the implantation of the Medtronic CoreValve PAV in a failing aortic bioprosthesis. In addition, the study aims to evaluate the performance and the safety of the implantation of the Medtronic CoreValve PAV in a failing aortic bioprosthesis at subsequent annual follow-ups out to 48 months post procedure. These objectives will be achieved through the following endpoints:

• Primary safety endpoint - Composite of Major Adverse Events
• Primary performance endpoint - Technical and procedural success at discharge Patient Population: Eligible subjects will be at least 75 years old, presenting with a failing aortic bioprosthesis (stenotic, incompetent or mixed) including homograft or stented or stentless heterograft, considered poor surgical candidates and necessitating repeat aortic valve replacement. Up to 20 patients will be included in up to four hospitals.

Conditions

Aortic Valve Stenosis

Outcome Measures

Primary Outcomes (2)

• Percentage of MAE Free Subjects

  Percentage of subjects without a composite major adverse event (MAE) at 30 days post procedure. the composite MAE includes: 1. MACCE (Major Adverse Cardiac or Cerebral Event): cardiac death, documented Mobitz type II second degree and third degree atrioventricular block, neurological events and surgical aortic valve replacement. 2. MAE: non cardiac death including sudden unexpected or unexplained death, cardiac tamponade, nonstructural valve dysfunction resulting in stenosis or regurgitation at the study valve not intrinsic to the valve itself, structural valve deterioration cardiogenic shock, operated valve endocarditis, valve thrombosis, aortic dissection/perforation, major bleeding event, peripheral embolic event and emergent revascularization procedure.

  30 days post-procedure

• Technical Success.

  The number of subjects in whom technical success was achieved where technical success was defined based on the device functionality as judged by the investigator adressing the ability of the system (1) to access the failing bioprosthetic valve via a peripheral vessel with the delivery catheter and (2) to deploy the valve accurately across the failing bioprosthetic valve and (3) to remove intact delivery system.

  30 days post procedure

Study Arms (1)

CoreValve

EXPERIMENTAL

Device: Medtronic CoreValve System

Interventions

Medtronic CoreValve System DEVICE

Transcatheter Aortic Valve

Also known as: Medtronic CoreValve Transcatheter aortic valve, Medtronic CoreValve Percutaneous aortic valve

CoreValve

Eligibility Criteria

• Age: 75 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Older Adult (65+)

You may qualify if:

• \> 74 years old,
• Symptomatic failing bioprosthetic aortic valve (stenotic, incompetent or mixed) confirmed by Doppler echocardiography,
• Logistic EuroSCORE \> 15%, or
• Any of the following criteria:
• Left ventricular ejection fraction (LVEF) \< 20%,
• Creatinine clearance \< 20mL/min (estimation using the Cockcroft calculation),
• Renal failure requiring dialysis,
• Permanent and long lasting (\> 6 month duration) atrial fibrillation,
• Cirrhosis of the liver (Child class A or B),
• Respiratory impairment (FEV1 \< 1L),
• Previous cardiac surgery (i.e., CABG especially if patient had competent mammary arteries on left anterior descending (LAD) artery or occluded saphenous veins with high-risk of coronary embolism during re-operation),
• Pulmonary hypertension ³ 60mmHg,
• Recurrent pulmonary embolus,
• Moderate tricuspid (\< grade 2+) insufficiency,
• Any severe disease contraindicating surgery,

You may not qualify if:

• Known hypersensitivity or contraindication to aspirin, heparin, ticlopidine and clopidogrel, Nitinol, or sensitivity to contrast media which cannot be pre-medicated,
• Active infection or endocarditis,
• Any intra left ventricular mass, thrombus or vegetation evidenced by Doppler echocardiography,
• Mitral or tricuspid valvular insufficiency ³ grade 2+,
• Prosthetic mitral or tricuspid valve,
• Femoral and/or iliac and/or aortic vascular condition (stenosis, occlusion or tortuosity) that could complicate endovascular access to the aortic valve bioprosthesis,
• Symptomatic carotid or vertebral artery narrowing (\> 70%) disease,
• Aortic abdominal or thoracic aneurysm,
• Bleeding diathesis or coagulopathy, or patient refuses blood transfusion,
• Active peptic ulcer or has had upper gastrointestinal bleeding within the past 3 months before baseline,
• Moribund status or cachexia with short life-expectancy independent of cardiac condition,
• Any acute neurological event or dysfunction occurred in the past 6 weeks before baseline or patient with severe senile dementia,
• Therapeutic invasive cardiac procedure, other than balloon aortic valvuloplasty, performed within 30 days prior to study procedure or to be performed during or within 30 days after the study procedure,
• Currently, enrolled in this study or another investigational drug or device study.

Sponsors & Collaborators

• Medtronic Cardiac Rhythm and Heart Failure: lead

Study Sites (3)

Herzzentrum Leipzig GmbH

Leipzig, Germany

Location

Deutsches Herzzentrum München

München, Germany

Location

Erasmus MC

Rotterdam, Netherlands

Location

Related Links

• Related Info

MeSH Terms

Conditions

Aortic Valve Stenosis

Condition Hierarchy (Ancestors)

Aortic Valve Disease; Heart Valve Diseases; Heart Diseases; Cardiovascular Diseases; Ventricular Outflow Obstruction

Results Point of Contact

• Title: M. Hollander
• Organization: Medtronic

maarten.hollander@medtronic.com

+31620534428

Study Officials

• E. Grube, Prof. Dr.

  Helios Heart Center Siegburg, Germany

  PRINCIPAL INVESTIGATOR

• G. Schuler, Prof. Dr.

  Universitat Leipzig Herzzentrum, Germany

  PRINCIPAL INVESTIGATOR

• R. Lange, Prof. Dr.

  Deutsches Herzzentrum Munich, Germany

  PRINCIPAL INVESTIGATOR

• P. de Jaegere, Dr.

  Erasmus MC Rotterdam, Netherlands

  PRINCIPAL INVESTIGATOR

Publication Agreements

• PI is Sponsor Employee: No
• Restrictive Agreement: No

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: January 15, 2010
• First Posted: January 18, 2010
• Study Start: June 1, 2008
• Primary Completion: January 1, 2010
• Study Completion: January 1, 2011
• Last Updated: January 31, 2019
• Results First Posted: January 31, 2019

Record last verified: 2018-08

Locations

DE (2); NL (1)