Flow-Controlled Ventilation to Improve Postoperative Pulmonary Outcome After Thoracic Surgery
NCT07623395
Mechanical Ventilation, Postoperative Pulmonary Complications (PPCs)
Sankt Gallen, Canton of St. Gallen, Switzerland
View Trial DetailsNCT Number: NCT07806188
This retrospective cohort study will include 412 adults mechanically ventilated >24 hours in intensive care unit in sohag university hospital between 2024 and 2026). Participants will be assigned to either, EGDS group ( equal to 208 ) or conventional sedation group (equal to 204 ). The main endpoint will be measured is the incidence of delirium in ICU , measured by the Confusion Assessment Method for the ICU (CAM-ICU). Secondary endpoints will be the number of the days free from ventilation at 28 days (VFDs), ICU length of stay (LOS) in the ICU, and the death during hospitalization.
Trial opening soon.
Get Notified18 year and older
All sexes
Observational
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Within 12 hours of intubation
main end point: occurrence of delirium during the ICU admission , defined as at least one positive CAM-ICU assessment.
Time frame: 6 months
Time frame: 6 months
Sohag University
Other
Dexmedetomidine for Sedation in Patients Requiring Mechanical Ventilation is Associated With a Lower Incidence of Delirium : A Retrospective Study
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