About this trial
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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Consecutive adult patients aged 18 years or older who required invasive mechanical ventilation for more than 24 hours.
Disqualifiers
Neurological primary admission such as stroke or traumatic brain injury.
Active seizures or alcohol withdrawal at admission.
Prior dementia or severe cognitive impairment.
Mechanical ventilation <24 hours.
Trial population
this retrospective observational trial was conducted in a 40-bed intensive care unit at sohag university hospital between January 2024, to ,march 2026. The Institutional Review Board granted approval for the trial protocol and informed consent was waived
Trial design
Other
Retrospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
occurrence of delirium during the ICU admission
main end point: occurrence of delirium during the ICU admission , defined as at least one positive CAM-ICU assessment.
Secondary outcomes
Number of Ventilator-free days (VFDs)
duration of ICU stay (LOS)
Locations
Sponsors and contacts
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