Aortic Valve Stenosis Clinical Trial
Official title:
Clinical Cohort Study - Hamburg AoRtic Valve cOhoRt
The primary aim of the study is to identify the optimal treatment modality for patients with aortic valve disease, incorporating the individual patient's risk profile and anticipated clinical outcomes. This includes the association of demographic factors, procedural data and biomarkers with clinical outcome in a prospective fashion.
Patients with severe aortic valve disease have a poor prognosis under medical therapy, making
replacement of the failing valve the preferred option. In addition to surgical aortic valve
replacement (SAVR), transcatheter aortic valve implantation (TAVI) has evolved as an
alternative treatment option for patients at intermediate and high operative risk. Before
expansion of TAVI to low-risk and younger patients can be recommended, several questions
remain to be investigated, e.g. optimal patient selection, periprocedural complications and
long-term durability. Therefore every patient with a relevant aortic valve disease (aortic
stenosis, aortic regurgitation or degenerative aortic valve prosthesis) who meets the
inclusion/exclusion criterias is planned to be involved in the study.
Predictors of outcome are yet to be defined in patients with aortic valve disease in order to
improve risk prediction for the different treatment modalities (medical, SAVR, TAVI).
The primary aim of the study is to identify the optimal treatment modality for the individual
patient, incorporating the individual patient's risk profile and anticipated clinical
outcomes. This includes the association of demographic factors, procedural data and
biomarkers with clinical outcome in a prospective fashion.
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|---|---|---|---|
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