Influence of intraoperative suggestions on postoperative development of delirium in patients undergoing TAVI procedure

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00024444

Enrollment

140

Registered

2021-09-17

Start date

2021-03-01

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

postoperative delirium

Interventions

Group 1: Following informed consent patients undergo a neurocognitive examination using the MMSE. A MMSE > 10 disqualified for study participation. The study is a randomized double blinded study. Fol

Eligibility

Sex/Gender

All

Age

18 Years to 110 Years

Inclusion criteria

Inclusion criteria: Patienten undergoing transfemoral aortic valve replacementKlappenersatz unterziehen müssen, age > 18 years, no diagnosis of dementia

Exclusion criteria

Exclusion criteria: severe brain damage due to Apoplexie or inrtacranial heorrhage, with cognitive decline and a MMSE s < 10 points, worde postoperative prognosis, procedure on ECMO, skin disease

Design outcomes

Primary

Measure	Time frame
The development of postoperative delirium.	—

Secondary

Measure	Time frame
postoperative analgetic requirement discharge from ICU Discharge from hospital sex difference	—

Countries

Germany

Contacts

Public ContactBarbara Sinner

Medizinische Universität Innsbruck, Klinik für Anästhesie und Intensivmedizin

barbara.sinner@i-med.ac.at0043 512 0504 38503

Outcome results

None listed

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