About this trial

This study aims to assess the association between perioperative cognitive function and postoperative quality of recovery.

Eligibility criteria

Qualifiers

elective non-cardiac surgery

age ≥65 years

duration of surgery ≥60 years

Disqualifiers

inability to give informed consent

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

140 Participants
are grouped into 1 trial group

Locations

This trial has no locations

Sponsors and collaborators

Universitätsklinikum Hamburg-Eppendorf

Lead sponsor