F05.8 F05.9
Conditions
Interventions
Group 1: Midazolam/Fentanyl vesus Methohexital/Fentanyl
Group 2: Propofol/Remifentanil versus Methohexital/Remifentanil
Sponsors
Abt. f. Anästhesie und Perioperative Medizin, Asklepios Klinik Langen
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: All ventilated and sedated patients aged > 18 years
Exclusion criteria
Exclusion criteria: Aged < 18 years, known neurological or psychiatrical diseases, any diseases making communication impossible
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| VAS, RASS und ICDSC every 8 h during the stay on the ICU. Primary end point: ICDSC-points during ICU stay. Nullhypothesis: there is no significant difference in the incidence of delirium measured with the ICDSC between Midazolam/Fentanyl vs. Methohexital/Fentanyl and Propofol/Remifentanil vs. Methohexital/Remifentanil. | — |
Secondary
| Measure | Time frame |
|---|---|
| Duration of mechanical ventilation, length of stay in ICU and hospital, mortality. Other variables: American Society of Anesthesiologists Classification (ASA), age, heigth, weight, sex, smoking status; SOFA, SAPS II, TISS 28 score; incidence of acute renal failure (RIFLE-criteria), numbers of interventions. | — |
Countries
Germany
Contacts
Public ContactHans-Bernd Hopf
Abt. f. Anästhesie und Perioperative Medizin, Asklepios Klinik Langen
Outcome results
None listed