Status:
RECRUITING
Identification of Outcome Relevant Indicators in Routine Data
Lead Sponsor:
Charite University, Berlin, Germany
Conditions:
Anesthesiological Risk Reduction
Intensive Care Risk Reduction
Eligibility:
All Genders
Up to 120 years
Brief Summary
The availability of electronic documentation systems in patient care means that large amounts of clinical routine data are available from which conclusions can be drawn for improving patient care. Com...
Detailed Description
The patterns that are relevant for patient-centered outcomes can be combinations of different parameters (e.g. vital signs, laboratory values, previous illnesses), which in themselves do not necessari...
Eligibility Criteria
Inclusion
- Age: 0 to 120 years
- Gender: female, male, diverse
- Electronically documented anesthesiological or intensive care treatment in the HIS (Hospital Information System) and PDMS (Patient Data Management System) of the Charité (Department of Anesthesiology and Intensive Care Medicine, CCM/CVK/CBF) since 2016
Exclusion
- none
Key Trial Info
Start Date :
December 3 2020
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
December 31 2026
Estimated Enrollment :
1000000 Patients enrolled
Trial Details
Trial ID
NCT04670744
Start Date
December 3 2020
End Date
December 31 2026
Last Update
December 24 2025
Active Locations (1)
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1
Department of Anesthesiology and Intensive Care Medicine (CCM/CVK), Charité - Universitaetsmedizin Berlin
Berlin, State of Berlin, Germany, 10117