Observational Study on Intubation Induction Agents in Critically Ill Patients
This study is looking back at medical records of critically ill adult patients who needed a breathing tube (tracheal intubation) in the surgical intensive care unit (ICU). Researchers want to understand if the choice of medicine used to help patients relax for intubation, like Propofol, affects how well they do. They are specifically looking at how many patients pass away within 7 days after intubation. You could be included if you are 18 or older, were admitted to the surgical ICU, received one of the studied induction agents, and have complete medical records. This is an observational study, meaning researchers are just reviewing existing information, not giving new treatments. The study aims to enroll 4 participants, but its current status is unclear.
- Study design
- This is an observational study, meaning researchers are looking back at existing medical records. It is not a clinical trial where new treatments are given.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- Researchers will look at outcomes for 7 days following tracheal intubation.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Induction Agent Choice With Early Mortality and Prognostic Outcomes in Critically Ill Patients
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- TOLGA SARAÇOĞLU, Prof,MD · PRINCIPAL_INVESTIGATOR · Florida University Jacksonville
Who to contact
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Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- Primary Outcome will be all-cause mortality at day 7 following tracheal intubationday 7
mortality at day 7