J90
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: • Admission to an intensive care unit • Evidence of pleural effusion (unilateral / bilateral) • No contraindications for the usage of the EIT belt • Patients receive EIT monitoring to monitor their ventilation, monitor their weaning process or monitor non-invasive ventilation.
Exclusion criteria
Exclusion criteria: • No pleural effusion detectable • Immobilization (e.g. unstable spinal trauma / ribs / Sternal fractures, pelvic fractures, etc.) prohibit the use of a belt for the EIT measurement • Patients with a pacemaker, cardioverter (ICD) or other electrical pacemakers, which are powered by the alternating current of the EIT measurement could be impaired in its function. • Patients with skin lesions in the area of the EIT belt location.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| - Quantification of pleural effusion with ultrasound or computed tomography - Quantification of pleural effusion after drainage (open surgical or via puncture) | — |
Secondary
| Measure | Time frame |
|---|---|
| - Detection of a “residual” pleural effusion despite drainage - Quantification of pleural effusion after drainage (osurgical drainage or drainage via puncture) via ultrasound | — |
Countries
Germany
Contacts
Klinik für Anästhesiologie und Operative Intensivmedizin, Uniklinikum Köln;"Studiensponsor" Qualitaetssicherung fuer klinische Studien, Prodekanat Wissenschaft der Medizinischen Fakultaet, Zentrum fuer klinische Studien Koeln