About this trial
Data on prevention of perioperative neurocognitive disorders (pNCDs) are limited. The purpose of this monocentric parallel - grouped observational registry is to collect study data from studies with pNCDs as primary or secondary endpoint to estimate prevalence and incidence of pNCDs.
Eligibility criteria
Qualifiers
Age 18 -100 years
Male or female patients undergoing elective surgery expected to last at least 60 min, screened at the Department of Anesthesiology and Operative Intensive Care Medicine (CCM, CVK), Charité - Universitätsmedizin Berlin, Berlin, Germany
Written informed consent to participate after having been properly instructed
Disqualifiers
Lacking willingness to take part in the study, or to have relevant study data collected, saved and analyzed for the purpose of the study
Accommodation in an institution due to an official or judicial order
Insufficient knowledge of German language
Members of the hospital staff
Trial design
Treatments tested in this trial
- Not listed