Aortic Valve Stenosis and/or Insufficiency Clinical Trial
Official title:
Post-Approval Study for the MOSAIC® Bioprostheses: A Long Term Follow Up Study.
A Single Center Non-Interventional Post-Market Release, Long Term Follow Up study of patients who underwent Isolated Aortic Valve Replacement or Isolated Mitral Valve Replacement with a Medtronic Mosaic Bioprosthesis. The purpose of this study is to evaluate the long term safety, efficacy and clinical performance of the Mosaic Bioprostheses.
Objectives:
The primary objectives of this study are to evaluate the long-term safety, efficacy and
clinical performance.
Study Design:
This is a prospective, single center, non-interventional, non-randomized, post-market release
clinical study
Sample Size and Study Duration:
A total of 255 patients had aortic valve replacement and 47 patients had mitral valve
replacement in the Albertinen-Krankenhaus (Hamburg, Germany) during the previous Mosaic
Pre-Market approval (PMA) study.
All surviving patients from the Mosaic Pre-Market Approval study at this center, will be
invited to participate. Approximately 225 patients will be invited.
This study is intended to serve as an ongoing source of information on long-term durability
and safety of the CE-marked Medtronic Mosaic bioprosthesis. As such the study is to continue
indefinitely until the last follow-up visit (until patient study exit due to patient death,
withdrawal of patient consent,...) of the last study patient.
PATIENT SELECTION:
Inclusion criteria:
- All patients who were enrolled and implanted with the Mosaic bioprosthesis in the
Albertinen-Krankenhaus (Hamburg, Germany) during the previous Mosaic PMA study, will be
invited to participate in this long- term follow-up study.
- Patients who are able to provide informed consent
Exclusion criteria:
- Patients who are not from the Albertinen-Krankenhaus (Hamburg, Germany) and who did not
participate in the Mosaic PMA study are ineligible for this study.
- Patients refusing or not able to provide informed consent.
- Patients not willing and unable to comply with the Clinical Investigation Plan
(CIP)-requirements.
Data Requirements and analysis:
For each patient enrolled in the study, information will be collected annually. Data will be
collected on the patient status and device hemodynamic performance by echocardiography.
Patient identity is anonymized.
Appropriate statistical analysis will be performed for the collected clinical data.
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