Observational Study of Prosthetic Tissue Aortic and Mitral Heart Valve

Not Applicable

Completed

• Conditions: Valvular Heart Disease

• Registration Number: NCT00329667
• Lead Sponsor: Abbott Medical Devices

Brief Summary

This study is a multi-center, prospective, non-randomized, observational study. The objectives of this study are to confirm the clinical safety and efficacy of the SJM Epic valve.

Detailed Description

This study is a multi-centered, multi-country, prospective, non-randomized, observational study, without concurrent or matched controls, conducted under a common protocol. Bayesian methods will be used for the design and analysis of this study. The Bayesian model will determine if the data for the valve configurations are poolable. Bayesian methods also provide a means of determining the appropriate stopping time for the study based on the amount of information generated. The objectives of this study are to confirm the clinical safety and efficacy of the SJM Epic Valve by establishing the following:

* adverse effect rates

* clinical status as indicated by NYHA functional classification

* hemodynamic performance

Study Timeline

• Study Start: 2003-01
• Primary Completion: 2006-03
• Study First Submitted: 2006-05-23
• Study First Submitted QC: 2006-05-23
• Study First Posted: 2006-05-25
• Study Completion: 2008-09
• Status Verified: 2019-02
• Last Update Submitted: 2019-02-01
• Last Update Posted: 2019-02-04

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 761

Inclusion Criteria

• The patient requires replacement of the aortic and/or mitral valve (Note: Patients undergoing concomitant procedures, e.g. coronary artery bypass grafting, valve repair, are eligible for this study).
• The patient (or legal guardian) has signed a study-specific informed consent, agreeing to the data collection and follow-up requirements.
• The patient is of legal age in host country.

Exclusion Criteria

• Patient already has a prosthetic valve, other than the aortic and/or mitral valve being replaced at this time.
• The patient requires replacement of the tricuspid or pulmonary valve.
• The patient is pregnant or nursing.
• Patient has active endocarditis.
• Patient is actively participating in the study of an investigational drug or device.
• Patient has had an acute preoperative neurological event.
• The patient is undergoing renal dialysis.
• Patient is an intravenous drug abuser, alcohol abuser or prison inmate.
• Patient has an inability or unwillingness to return for the required follow-up intervals.
• The patient had the SJM Epic Valve implanted during the clinical study but then had the bioprosthesis explanted.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Hemodynamic performance	At required follow-up visits
Adverse effect rates	Ongoing
Clinical status as indicated by NYHA functional classification	At required follow-up visits