Functionality and Outcome in Older Patients with severe Aortic Stenosis

Recruiting

• Conditions: I35.0; Aortic (valve) stenosis

• Registration Number: DRKS00012494
• Lead Sponsor: Klinikum NürnbergParaceslus Medizinische Privatuniversität

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2017-06-08
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 150

Inclusion Criteria

Older adults aged over 75 years with isolated severe aortic stenosis
Agreement of the patient

Exclusion Criteria

Missing patient consent
Combined aortic valve disease
Limited life expectancy of approximately twelve months

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
functionality (using Geriatric Assessment), mortality, cardiovascular mortality, quality of life (using EuroQol-5D)<br>time points:<br>preoperative<br>perioperative<br>at 3 months<br>at 12 months<br>

Secondary Outcome Measures

Name	Time	Method
complications, cardiovascular complications