About this trial

This prospective, multicenter observational registry systematically captures all emergency department tracheal intubations across participating hospitals in Taiwan. The registry focuses on process quality indicators, including first-pass success, and patient-safety outcomes, including hypoxemia, hypotension, and peri-intubation cardiac arrest within 30 minutes of intubation. Routinely generated laboratory and physiologic variables are also collected to improve risk stratification and identify predictors of major adverse events. The study is non-interventional and does not alter clinical care.

Eligibility criteria

Qualifiers

Undergoing tracheal intubation in the emergency department during the study period

Disqualifiers

Prehospital intubation; intubation performed solely for elective anesthesia/procedural sedation outside emergency indications

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

1,200 Participants
are grouped into 1 trial group

Locations

1
New Taipei Municipal Tucheng Hospital, New Taipei City, Taiwan New Taipei City Taiwan

Sponsors and collaborators

Chang Gung Memorial Hospital

Lead sponsor