Predictors of postoperative delirium - a pilot study.
Recruiting
- Conditions
- F50.8Other eating disorders
- Registration Number
- DRKS00031157
- Lead Sponsor
- Private Universität Witten/Herdecke gGmbh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 150
Inclusion Criteria
elective surgery, with expected duration of =60 minutes, without expected stay in intensive care unit (ICU)
Exclusion Criteria
Diagnosed dementia or other chronic neurological/neuropsychiatric disease.
- Acute central nervous system disorders (e.g., traumatic brain injury, intracranial hemorrhage, encephalitis, meningitis)
-severe sepsis and septic shock
-Intoxications
-intracranial surgery
-expected length of hospital stay <3 days
-German not as native language
-deafness
- Emergency surgery
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method POD until postoperative day 3/discharge. If needed, POD will be treated; this treatment will be at the discretion of the physician(s) according to hospital standards and is not part of this study.
- Secondary Outcome Measures
Name Time Method in-house mortality; postoperative complications; morbidity (Dindo Clavien Classification); nausea/vomiting; pre- to postoperative course of MMSE/hand strength; morbidity/cognitive performance at 3-month follow-up.