---
title: Prospective Assessment Project of AirwaY Management-related Incidents in Adult Anaesthesia Care PAPAYA III
nct_id: NCT06117176
overall_status: RECRUITING
sponsor: Insel Gruppe AG, University Hospital Bern
study_type: OBSERVATIONAL
primary_condition: Airway Complication of Anesthesia
countries: Germany, Switzerland
canonical_url: "https://parkinsonspathways.com/agent/trials/NCT06117176.md"
clinicaltrials_gov: "https://clinicaltrials.gov/study/NCT06117176"
ct_last_update_post_date: 2026-03-04
last_seen_at: "2026-05-12T06:01:53.514Z"
source: ClinicalTrials.gov (mirrored, no enrichment)
---
# Prospective Assessment Project of AirwaY Management-related Incidents in Adult Anaesthesia Care PAPAYA III

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

**NCT ID:** [NCT06117176](https://clinicaltrials.gov/study/NCT06117176)

## Key Facts

- **Status:** RECRUITING
- **Study Type:** OBSERVATIONAL
- **Target Enrollment:** 40000
- **Lead Sponsor:** Insel Gruppe AG, University Hospital Bern
- **Collaborators:** University of Bern, University of Lausanne Hospitals, Kantonsspital Aarau, Charite University, Berlin, Germany, Universitätsklinikum Hamburg-Eppendorf
- **Conditions:** Airway Complication of Anesthesia, Adverse Events
- **Start Date:** 2025-02-01
- **Completion Date:** 2027-03
- **CT.gov Last Update:** 2026-03-04

## Brief 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.

## Detailed Description

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.

## Eligibility

- **Minimum age:** 18 Years
- **Sex:** ALL
- **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 Outcomes

- **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

- **The Incidences of the individual major incidents** _(time frame: 30 days)_
- **The Incidences of the individual minor incidents** _(time frame: 30 days)_

## Locations (5)

- 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, Switzerland — _RECRUITING_
- Kantonsspital Aarau, Aarau, Switzerland — _NOT_YET_RECRUITING_
- CHUV Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland — _NOT_YET_RECRUITING_

## Recent Field Changes (last 30 days)

- `status.overallStatus` — added _(2026-05-12)_
- `status.primaryCompletionDate` — added _(2026-05-12)_
- `status.completionDate` — added _(2026-05-12)_
- `status.lastUpdatePostDate` — added _(2026-05-12)_
- `design.enrollmentCount` — added _(2026-05-12)_
- `eligibility.criteria` — added _(2026-05-12)_
- `eligibility.minAge` — added _(2026-05-12)_
- `eligibility.sex` — added _(2026-05-12)_
- `outcomes.primary` — added _(2026-05-12)_
- `outcomes.secondary` — added _(2026-05-12)_
- `sponsor.lead` — added _(2026-05-12)_
- `sponsor.collaborators` — added _(2026-05-12)_
- `results.hasResults` — added _(2026-05-12)_
- `locations.deutsches herzzentrum der charité and charité|berlin||germany` — added _(2026-05-12)_
- `locations.universitätsklinikum hamburg-eppendorf|hamburg||germany` — added _(2026-05-12)_
- `locations.inselspital, bern university hospital|bern|canton of bern|switzerland` — added _(2026-05-12)_
- `locations.kantonsspital aarau|aarau||switzerland` — added _(2026-05-12)_
- `locations.chuv centre hospitalier universitaire vaudois|lausanne||switzerland` — added _(2026-05-12)_

---

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*Source data (authoritative): https://clinicaltrials.gov/study/NCT06117176*  
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