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Prospective evaluation of adverse events during neonatal endotracheal intubations

Prospective evaluation of adverse events during neonatal endotracheal intubations - PREVENT

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00013575
Enrollment
93
Registered
2017-12-29
Start date
2017-09-16
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Respiratory insufficiency in preterm and term babies

Interventions

Group 1: Newborn babies who are intubated during birth hospitalization are prospectively recorded. The main objective of the study is to record any adverse events associated with intubation (e.g. brad

Sponsors

Zentrum für Kinder- und Jugendmedizin Universitätsmedizin Mainz, Abteilung Neonatologie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 12 Months

Inclusion criteria

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

Exclusion criteria: - incomplete documentation (primary endpoint can not be determined), - patient has previously been discharged home

Design outcomes

Secondary

MeasureTime frame
Importants secondary endpoints are: tube insertion depth, time of the procedure and the number of attempts until succesful intubation.

Primary

MeasureTime frame
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.

Countries

Germany

Contacts

Public ContactSusanne Tippmann

Zentrum für Kinder- und Jugendmedizin Universitätsmedizin Mainz, Abteilung Neonatologie

Susanne.Tippmann@unimedizin-mainz.de06131175890

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026