Prospective evaluation of adverse events during neonatal endotracheal intubations
Recruiting
- Conditions
- Respiratory insufficiency in preterm and term babies
- Registration Number
- DRKS00013575
- Lead Sponsor
- Zentrum für Kinder- und Jugendmedizin Universitätsmedizin Mainz, Abteilung Neonatologie
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 93
Inclusion Criteria
live birth
- Intubation by the staff of the neonatal intensive care unit in the delivery room of the perinatal center of the University Medical Center Mainz, in the neonatal intensive care unit or in Katholisches Klinikum Mainz as part of the postnatal emergency care
Exclusion Criteria
- incomplete documentation (primary endpoint can not be determined), - patient has previously been discharged home
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary endpoint is the detection of adverse events associated with intubations in neonatology. Adverse events are recorded via checklists, including inter alia: cardiac arrest, bradycardia, hypoxemia, airway injury, and intubation of the esophagus.
- Secondary Outcome Measures
Name Time Method Importants secondary endpoints are: tube insertion depth, time of the procedure and the number of attempts until succesful intubation.