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

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

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00031805

Enrollment

1200

Registered

2023-05-03

Start date

2023-05-04

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

I35.0

Interventions

Group 1: Patient cohort - Data collection: Baseline (pre-TAVI), 30 days post-TAVI, 1 year post-TAVI - Prospective follow-up (observational) over up to 10 years

Eligibility

Sex/Gender

All

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

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

Secondary

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

Countries

Germany

Contacts

Public ContactUte Mons

Uniklinik Köln

ute.mons@uk-koeln.de+49 221 478 85610

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026