Status:
UNKNOWN
Estimation of Delirium Data Completeness
Lead Sponsor:
Efficacy Care R&D Ltd
Collaborating Sponsors:
Hadassah Medical Organization
Conditions:
Delirium
Delirium Drug-Induced
Eligibility:
All Genders
18-90 years
Brief Summary
Currently physicians and nurses rely on their own clinical skills and experience to diagnose and record 'delirium' in the Electronic Health Records (EHR). This study aims to determine how delirium as ...
Detailed Description
Clinical Background:: Postoperative encephalopathy known as "delirium" is a deleterious, potentially risky, and often preventable complication representing a serious "brain failure" condition, common...
Eligibility Criteria
Inclusion
- All postoperative patients aged 18 years and older; and
- Undergoing unplanned admission to an intensive care unit (ICU); or
- Major complications associated with either operating room procedure or anesthesia. Example: Cardiac or circulatory event and/or Cardiac arrest during or within 24 hours of operation or administration of anesthesia; or Acute myocardial infarction (AMI) during or within 48 hours of operation or administration of anesthesia; or
- Postoperative Central Nervous System (CNS) event (e.g., CVA, seizures, coma) during or within 48 hours of operation or administration of anesthesia; AND
- Respiratory failure not present prior to the 25th hour of hospitalization or not present before surgery;
Exclusion
- Delirium present on admission; or
- any psychotic or degenerative related diagnosis on admission (e.g. Senile and presentile dementias such as Alzheimer's or Pick's dementia, Creutzfeldt-Jakob disease, Huntington's chorea, Wilson's disease).
Key Trial Info
Start Date :
October 1 2019
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
November 1 2020
Estimated Enrollment :
50000 Patients enrolled
Trial Details
Trial ID
NCT04084821
Start Date
October 1 2019
End Date
November 1 2020
Last Update
September 10 2019
Active Locations (1)
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1
Haddasah Medical Center
Jerusalem, IL, Israel