J80.0 A41.9 R57.2 J18
Conditions
Interventions
Group 1: Intensive care patients with ARDS, pneumonia, sepsis and septic shock. In this study, the mobilization of ICU patients will be observed and compared to a mobilization algorithm (observational
Sponsors
Charité Campus Virchow-Klinikum
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Diagnosis: sepsis, septic shock, ARDS or pneumonia
Exclusion criteria
Exclusion criteria: • Patients with polytrauma or traumatic brain injury • Patients with intracranial or intrathoracical surgery • infaust prognosis (death expected within the next hours) • pregnant or breastfeeding patients • patient is placed in a penal institution • consent cannot be obtained by legal proxy • patients advance directives exclude participation in a trial
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of the physician prescribed level of mobilization with the algorithm based recommendation | — |
Secondary
| Measure | Time frame |
|---|---|
| • Evaluation of the current state of early ICU mobilization • Evaluation of safety of the mobilization algorithm • If necessary further development of the algorithm • Identification of risk factors leading to adverse events or termination of early mobilization | — |
Countries
Germany
Contacts
Public ContactSteffen Weber-Carstens
Charité - Universitätsmedizin Berlin, Campus Virchow-Klinikum, Klinik für Anästhesiologie und Intensivmedizin
Outcome results
None listed