Identification of Outcome Relevant Indicators in Routine Data
Recruiting
Observational Study
Anesthesiological Risk Reduction
Intensive Care Risk Reduction
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- Up to 120
- Sex
- Any
- Study type
- Observational
- Participants needed
- 1,000,000 (estimated)
- Sponsor
- Charite University, Berlin, Germany · Other
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About This Trial
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. Compared to conventional research approaches, a data science-oriented approach offers the possibility of identifying patterns in routine data ("pattern recognition") that are relevant for patient-centere…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 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 Medi…
Contacts