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Clinical Trials/DRKS00017198
DRKS00017198
Recruiting
Not Applicable

Influence of an inhalative vs. intravenous sedation regimen on the spatial distributions of regional ventilation and transpulmonary pressures in mechanically ventilated patients - Lung function IsoPro

niversitätsklinik für Anästhesiologie, operative Intensivmedizin, Rettungsmedizin, Schmerztherapie, Campus OWL, Klinikum Herford AöR0 sites10 target enrollmentJuly 23, 2019
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ConditionsJ96.0Acute respiratory failure

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
J96.0
Sponsor
niversitätsklinik für Anästhesiologie, operative Intensivmedizin, Rettungsmedizin, Schmerztherapie, Campus OWL, Klinikum Herford AöR
Enrollment
10
Status
Recruiting
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 23, 2019
End Date
TBD
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
niversitätsklinik für Anästhesiologie, operative Intensivmedizin, Rettungsmedizin, Schmerztherapie, Campus OWL, Klinikum Herford AöR

Eligibility Criteria

Inclusion Criteria

  • •1\) Patients who have received intravenous sedation with propofol for at least 24 hours and
  • •2\) who require a change of sedation regime for clinical reasons.

Exclusion Criteria

  • •1\) pregnancy
  • •2\) minors \< 18 years old
  • •3\) allegies to propofol and/or isoflurane
  • •4\) susceptibility to malignant hyperthermia
  • •5\) application of tidal volumes \<200 ml
  • •6\) risk of increased intracranial pressure and no possibility of continuous ICP/CPP monitoring

Outcomes

Primary Outcomes

Not specified

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