Z51
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: All patients on critical care unit or in the operating room requiring a central venous catheter were included in the study after informed consent.
Exclusion criteria
Exclusion criteria: age <18 years participation in another study former participation in the same study missing informed consent patients with a legal representative permanently unable to give consent contraindication for central venous cannulation contraindication or refusal for a left sided subclavian central venous catheter emergency situation with unstable patients no proof of patency of the vessel during ultrasound prescan
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Risk Score (0-53) | — |
Secondary
| Measure | Time frame |
|---|---|
| Success rate Complications Infection score (0 to 4) Pucture site (distance to clavicle and jugular fossa) Number of skin punctures | — |
Countries
Germany
Contacts
Universitätsklinikum des SaarlandesKlinik für Anästhesiologie, Intensivmedizin und Schmerztherapie