Retrospective Evaluation of POCD Data of Studies From KAI, Charité - Universitätsmedizin Berlin
Recruiting now
Conditions studied: Postoperative Cognitive Dysfunction
In brief
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.
Key facts
- Study ID
- NCT02832193
- Run by
- Charite University, Berlin, Germany
- People needed
- 5000
- Starts
- 2009-03-01
- Expected to finish
- 2027-12-01
- Last updated by the study team
- 2025-11-26
Who can join
Age: 18 and older, up to 100. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- 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
You may not qualify if…
- 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
- Homelessness or other conditions that disable reachability for postoperative assessment by post or telephone
- Illiteracy
- Patients who had a history of neurologic deficits (e.g. stroke, history of seizures, etc.)
- Hearing impairment that severely affects the neuropsychological testing.
- Visual impairment that severely affects the neuropsychological testing.
- Participation in other prospective clinical interventional trials
- Control Group
- Inclusion Criteria:
- Age 18 - 100 years
- Male or female patients (ASA Status I, II+III)
- No planned surgery during the next 3 months
- No surgery during the past 6 months before study inclusion
- Written informed consent to participate after having been properly instructed
- Exclusion Criteria:
- Insufficient knowledge of German language Lacking willingness to take part in the study, or to have relevant study data collected, saved and analyzed for the purpose of the study
- Neuropsychiatric conditions that severely affect the neuropsychological testing
- Hearing impairment that severely affects the neuropsychological testing
- Visual impairment that severely affects the neuropsychological testing
Where it is running
- Department of Anesthesiology and Operative Intensive Care Medicine Berlin (CCM, CVK), Charité - Universitätsmedizin Berlin — Berlin, Germany (enrolling)
- Irmgard Landgraf — Berlin, Germany
Full record on ClinicalTrials.gov
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