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Clinical Trials in Germany / NCT06117176
Recruiting Observational

Prospective Assessment Project of AirwaY Management-related Incidents in Adult Anaesthesia Care PAPAYA III

NCT06117176 · tracked via the Priya Life Science Germany tracker
Phase
Observational
Started
2025-02-01
Last updated
2026-03-04

Condition(s) studied

Airway Complication of AnesthesiaAdverse Events

Study summary

The overall objective of the study is to evaluate and analyze major and minor incidents during airway management in adults under anaesthesia care at all study sites. The patient characteristics, type of airway management is recorded and if airway management-related incidents occur, they are analyzed in more detail to improve patient safety in the future.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * All adult patients requiring airway management under anaesthesia care for elective, semi-elective, urgent or emergency diagnostic procedures or interventions. Airway management includes awake and asleep tracheal intubation, insertion of supraglottic airway devices, and face mask ventilation. * Patients older than 18 years of age * Informed consent given or general consent in place, according to local ethics committee requirements. Exclusion Criteria: * Refusal to give consent or withdrawal of consent. * Patients \<18 years.

Primary outcome measure(s)

Trial sites (5)

FacilityCityRegionStatus
Deutsches Herzzentrum der Charité and Charité Berlin Germany Not Yet Recruiting
Universitätsklinikum Hamburg-Eppendorf Hamburg Germany Not Yet Recruiting
Inselspital, Bern University Hospital Bern Canton of Bern Recruiting
Kantonsspital Aarau Aarau Switzerland Not Yet Recruiting
CHUV Centre Hospitalier Universitaire Vaudois Lausanne Switzerland Not Yet Recruiting

More Insel Gruppe AG, University Hospital Bern trials in Germany

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06117176 on ClinicalTrials.gov ↗ ← All trials in Germany