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NCT Number: NCT06117176

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

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.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Deutsches Herzzentrum der Charité and Charité, Berlin, Germany

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About this study

It is a prospective observational cross-sectional European multi-centre study collecting health-related patient data on anaesthetic airway management over three months. This detects the incidence and nature of local airway management problems and assesses how they are solved. This will enable the investigators to identify generalisable interventions and recommendations to further improve patients' airway management to improve patient safety. During the observational period, the anaesthesia staff in charge will fill out a screening questionnaire for airway management for every patient undergoing anaesthesia care with airway management. The investigators will extract the characteristics from the local anaesthesia record system for all patients. If no event arises, there are no further requirements. If an event occurs, the anaesthesia provider will fill out an additional form asking for more details on what happened.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Primary outcomes

  1. Number of airway management related incidents

    Time frame: 30 days

    Primary study outcome is the number of anaesthesia cases with at least one airway management related incidents in adult patients under anaesthesia care.

Secondary outcomes

  1. The Incidences of the individual major incidents

    Time frame: 30 days

    Secondary study outcome parameters are the incidences of the major critical events and the number of incidents per case incidents.

  2. The Incidences of the individual minor incidents

    Time frame: 30 days

    Secondary study outcome parameters are the incidences of the minor critical events and the number of incidents per case incidents.

Study contacts

Contact information is provided by the study sponsor or research team.

Alexander Fuchs, MD

CONTACT

[email protected]

+41 31 664 14 65

Thomas Riva, MD,PD

CONTACT

[email protected]

+41 31 632 21 11

Sponsors and collaborators

Lead sponsor

Insel Gruppe AG, University Hospital Bern

Other

Collaborators

  • Charite University, Berlin, Germany
  • Kantonsspital Aarau
  • University of Bern
  • University of Lausanne Hospitals
  • Universitätsklinikum Hamburg-Eppendorf

Registry information

Official study title

Prospective Assessment Project of AirwaY Management-related Incidents in Adult Anaesthesia Care (PAPAYA III) - A European Multicentre Cross-sectional Observational Study

Acronym: PAPAYA-III

Important dates

Study start
2025
Primary completion
2026
Study completion
2027
First posted
Nov 3, 2023
Registry last updated
Mar 4, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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