Short- and long-term outcomes after TAVI - An epidemiological prospective patient cohort study

Recruiting

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

• Registration Number: DRKS00031805
• Lead Sponsor: niklinik Köln

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2023-05-03
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 1200

Inclusion Criteria

informed consent to participate in the study
- Receiving a TAVI at the Heart Centre of the University Hospital Cologne

Exclusion Criteria

- No informed consent for the study
- Receiving TAVI as an emergency measure
- Receiving other invasive procedures besides TAVI
- No sufficient German language skills

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Cardiovascular mortality (death from cardio- or cerebrovascular disease according to ICD-10/ICD-11 as per death certificate)

Secondary Outcome Measures

Name	Time	Method
Other prognostic outcomes (all-cause mortality, hospitalisations...) and biopsychosocial factors (cognition, depressiveness, functional status...)