Retrospective Evaluation of POCD Data of Studies From KAI, Charité - Universitätsmedizin Berlin

Recruiting Observational Study
Postoperative Cognitive Dysfunction
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 – 100
Sex
Any
Study type
Observational
Participants needed
5,000 (estimated)
Sponsor
Charite University, Berlin, Germany · Other
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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.

Trial Locations
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Eligibility Criteria
Study Group Inclusion Criteria: * 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…
Contacts

Claudia Spies, MD, Prof.

+49 30 450 5510 01

claudia.spies@charite.de

CONTACT