Hamburg AoRtic Valve cOhoRt

NCT04227002 · tracked via the Priya Life Science Germany tracker

Sponsor

Universitätsklinikum Hamburg-Eppendorf

Phase

Observational

Started

2019-09-01

Last updated

2020-01-13

Condition(s) studied

Aortic Valve Stenosis

Study summary

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.

Eligibility

Sex

ALL

Min age

18 Years

Max age

—

Healthy volunteers

Inclusion Criteria: * Patients with clinically relevant aortic valve disease (aortic valve stenosis, aortic regurgitation, degenerated aortic valve prosthesis) * Written informed consent Exclusion Criteria: * Insufficient knowledge of the German language (able to understand and write the German language) * Physical or psychological incapability to take part in the investigation

Primary outcome measure(s)

All cause mortality — one year
The primary aim of the study is to investigate all cause mortality after surgical aortic valve replacement or transcatheter aortic valve replacement. Events of death will be registered either from in-house information or telephone follow-up of the patient or the referring physician as part of clinical routine.

Trial sites (1)

Facility	City	Region	Status
Universitäres Herz- und Gefäßzentrum	Hamburg	Germany	Recruiting

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Other trials for the same condition

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04227002 on ClinicalTrials.gov ↗ ← All trials in Germany