Carpentier-Edwards PERIMOUNT Magna Ease Pericardial Bioprosthesis, Model 3300TFX

Not Applicable

Completed

• Conditions: Aortic Valve Disorder; Aortic Valve Insufficiency; Coronary Artery Disease; Aortic Valve Stenosis; Heart Failure

• Registration Number: NCT01171625
• Lead Sponsor: Edwards Lifesciences

Brief Summary

The purpose of the study is to demonstrate the long term safety and effectiveness of the Carpentier-Edwards PERIMOUNT Magna Ease Valves in patients undergoing aortic valve replacement with or without concomitant procedures requiring cardiopulmonary bypass.

Detailed Description

This is a prospective, single-arm, multi-center, interventional study to be conducted in the US and outside the US (OUS). This study will enroll a minimum of 225 patients implanted with the study valve in order to achieve 101 aortic valve replacement subjects each followed for a minimum of 8 years. The study will include male and female patients, 18 years or older, requiring replacement for a diseased, damaged or malfunctioning natural or prosthetic aortic valve. Patients will be followed and assessed after implant at discharge, 6 months, one year, and annually for a minimum of 8 years.

Study Timeline

• Study Start: 2007-10
• Study First Submitted: 2010-07-26
• Study First Submitted QC: 2010-07-27
• Study First Posted: 2010-07-28
• Primary Completion: 2018-09
• Study Completion: 2018-09
• Results First Submitted: 2020-02-06
• Status Verified: 2020-04
• Results First Submitted QC: 2020-04-07
• Last Update Submitted: 2020-04-07
• Results First Posted: 2020-04-17
• Last Update Posted: 2020-04-17

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 283

Inclusion Criteria

1. The patient requires, as indicated in the preoperative evaluation, a replacement aortic valve.
2. The patient is an average or better operative risk.
3. The patient is geographically stable and agrees to attend follow-up assessments at the hospital of surgical services for at least 8 years.
4. The patient is 18 years or older.
5. The patient has signed and dated the subject informed consent form prior to surgery.

Exclusion Criteria

1. The patient has any known non-cardiac life-threatening disease, which will limit the patient's life expectancy below 1 year.
2. The patient presents with active endocarditis within the last 3 months.
3. The patient has an abnormal calcium metabolism (e.g., chronic renal failure, hyperparathyroidism).
4. The patient has an aneurismal aortic degenerative condition (e.g., cystic medial necrosis, Marfan's syndrome).
5. The patient is pregnant or lactating.
6. The patient is an intravenous drug abuser.
7. The patient is currently a prison inmate.
8. The patient is currently participating in a study of an investigational drug or device.
9. The patient requires replacement of a native or prosthetic mitral, tricuspid or pulmonic valve.
10. The patient requires a repair of the mitral or tricuspid valve with the use of an annuloplasty device.
11. The patient was previously enrolled in the study.
12. The patient had a prior mitral, tricuspid or pulmonic valve surgery, which included implantation of a bioprosthetic valve, mechanical valve, or annuloplasty ring that will remain in situ.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Subject's Percentage of Long Term Safety Performance	31 days through 8 years post-implant	Long term safety performance will be evaluated by comparing the linearized yearly rates to the objective performance criteria (OPC) referenced in the Food and Drug Administration (FDA) 1994 Draft Heart Valve Guidance.; Expressed as the Number of late events divided by the total number of late patient years times 100. Late patient years are calculated from 31 days post-implant to the date of the last contact (follow up or adverse event).
Number of Subject's in NYHA Functional Class I or II at 8 Year Post-Implant	8 years post-implant	The New York Heart Association (NYHA) functional classification system relates symptoms to everyday activities and the patient's quality of life.; Class I. No limitation of physical activity. Ordinary physical activity does not cause undue fatigue, palpitation, dyspnea (shortness of breath).; Class II. Slight limitation of physical activity. Comfortable at rest. Ordinary physical activity results in fatigue, palpitation, dyspnea (shortness of breath).
Subject's New York Heart Association (NYHA) Functional Class at 8 Years Post-Implant Compared to Baseline	8 Years post-implant	The New York Heart Association (NYHA) functional classification system relates symptoms to everyday activities and the patient's quality of life.; Class I. No limitation of physical activity. Ordinary physical activity does not cause undue fatigue, palpitation, dyspnea (shortness of breath).; Class II. Slight limitation of physical activity. Comfortable at rest. Ordinary physical activity results in fatigue, palpitation, dyspnea (shortness of breath).; Class III. Marked limitation of physical activity. Comfortable at rest. Less than ordinary activity causes fatigue, palpitation, or dyspnea.; Class IV. Unable to carry on any physical activity without discomfort. Symptoms of heart failure at rest. If any physical activity is undertaken, discomfort increases.

Secondary Outcome Measures

Name	Time	Method
Percent of Early Adverse Events	Events occurring within 30 days of procedure	Number of early adverse events occurring within 30 days of procedure divided by the number of enrolled subjects times 100.
Percentage of Late Adverse Events	Events occurring >= 31 days and up through 8 years post-implant	Number of late events divided by the total number of late patient years times 100. Late patient years are calculated from 31 days post-implant to the date of the last contact (follow up or adverse event).
Percent of Subjects With Freedom From Serious Adverse Events (SAE) Post-implant > 30 Days	1 Year, 2 Years, 3 Years, 4 Years, 5 Years, 6 Years, 7 Years, and 8 Years post-implant	Subject's freedom from Serious Adverse Events at \> 30 days post-implant. Time to events were estimated by Kaplan-Meier method.
Subject's Average Peak Systolic Gradient (mmHg) Measurements at 8 Years Post-implant	8 years post-implant	Peak systolic gradient is the maximum value measured of flow of blood through the aortic valve as measured in millimeters of mercury. The data summary will be stratified by valve size.
Subject's Average Mean Systolic Gradient (mmHg) Measurements at 8 Years Post-implant.	8 years post-implant	Mean systolic gradient is the average flow of blood through the aortic valve measured in millimeters of mercury. Mean gradient values depend on the size and type of valve. The data summary will be stratified by valve size.
Subject's Average Effective Orifice Area Measurements at 8 Years Post-implant.	8 years post-implant	Effective orifice area represents the cross-sectional area of the blood flow downstream of the aortic valve. The data summary will be stratified by valve size.
Subject's Average Effective Orifice Area Index (EOAI) Measurements at 8 Years Post-implant.	8 years post-implant	Effective orifice area index represents the minimal cross-sectional area of the blood flow downstream of the aortic valve divided by the person's body surface area. The data summary will be stratified by valve size.
Subject's Average Performance Index Measurements at 8 Years Post-implant.	8 years post-implant	Performance index is defined as the subject's effective orifice area (the cross-sectional area of the blood flow downstream of the aortic valve) divided by the subject's native orifice area. The data summary will be stratified by valve size.
Subject's Average Cardiac Output Measurements at 8 Years Post-implant.	8 years post-implant	The amount of blood the heart pumps through the circulatory system in a minute. The data summary will be stratified by valve size.
Subject's Average Cardiac Index Measurements at 8 Years Post-implant.	8 years post-implant	Cardiac index is an assessment that divides the cardiac output from left ventricle in one minute by the person's body surface area (BSA), thus relating heart performance to the size of the individual. The data summary will be stratified by valve size.
Subject's Amount of Aortic Valvular Regurgitation at 8 Years Post-Implant.	8 years post-implant	Aortic valvular regurgitation occurs when the aortic valve in the heart does not close tightly allowing some of the blood that was pumped out of the heart to leak back into it. Aortic valvular regurgitation is evaluated by echocardiography over time. It is assessed on a scale from 0 to 4, where 0 represents no regurgitation and 4 represents severe regurgitation.
Subject's Average White Blood Cell Count Measurement Over Time.	6 months and annually for 8 years post-implant	Laboratory analysis of White Blood Cell Count on blood drawn from subject; WBC fight infection.
Subject's Average Red Blood Cells Count Over Time.	6 months and annually for 8 years post-implant	Laboratory Analysis of Red Blood Cell (RBC) Count on blood drawn from subjects; RBC carry oxygen.
Subject's Average Hematocrit Percentage Over Time.	6 months and annually for 8 years post-implant	Laboratory Analysis of Hematocrit Percentage on blood drawn from subjects. Hematocrit is the proportion of red blood cells to the fluid component (plasma) in the blood.
Subject's Average Platelet Count Over Time.	6 months and annually for 8 years post-implant	Laboratory Analysis of Platelet Count on blood drawn from subjects; platelets help with blood clotting.
Subject's Average Serum Lactate Dehydrogenase (LDH) Over Time.	6 months and annually for 8 years post-implant	Laboratory Analysis of Serum Lactate Dehydrogenase on blood drawn from subjects; The lactate dehydrogenase (LDH) test looks for signs of damage to the body's tissues.
Subject's Average Haptoglobin Measurement Over Time.	6 months and annually for 8 years post-implant	Laboratory Analysis of haptoglobin on blood drawn from subjects; haptoglobin is a protein produced by the liver.
Subject's Average Reticulocytes Percentage Over Time.	6 months and annually for 8 years post-implant	Laboratory Analysis of reticulocytes on blood drawn from subjects. Reticulocytes are newly produced immature red blood cells; a reticulocyte blood test measures the amount of these cells in the blood.
Subject's Average Score on the EQ-5D- Quality of Life Questionnaire at Baseline and 6 Months Post-Implant.	Baseline and 6 Months Post-Implant	The EQ-5D is a standardized questionnaire that asks subjects to rate themselves (no problems, some problems, extreme problems) on mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. The scale ranges from a minimum of 0 and a maximum of 100 where zero is the 'worst state imaginable' and 100 is the 'best state imaginable'.
Subject's Average Hemoglobin Count Over Time.	6 months and annually for 8 years post-implant	Laboratory Analysis of Hemoglobin Count on blood drawn from subjects. Hemoglobin is an oxygen-carrying protein in red blood cells.

Trial Locations

Locations (13)

Mercy General Hospital; 🇺🇸 Sacramento, California, United States

Cooper University Hospital; 🇺🇸 Camden, New Jersey, United States

Morristown Memorial Hospital; 🇺🇸 Morristown, New Jersey, United States

Providence Heart & Vascular Institute; 🇺🇸 Portland, Oregon, United States

St. Marks Hospital; 🇺🇸 Salt Lake City, Utah, United States

Universitatslinik fur Chirurgie; 🇦🇹 Innsbruck, Austria

Sunnybrook Health Sciences Centre; 🇨🇦 Toronto, Ontario, Canada

St. Paul's Hospital; 🇨🇦 Vancouver, Canada

Liknik fur Herz und BefaBchirurgie Im Deuschen Herzzentrum; 🇩🇪 Munich, Lazarettstr, Germany

Klinik fur Herz-, Thorax-, Transplantations- und Gefabchirurgie; 🇩🇪 Hannover, Germany

Scroll for more (3 remaining)