Structural Modification In Supraglottic Airway Device
NCT04498598
Airway Complication of Anesthesia, Hypoventilation
Cleveland, Ohio, United States
View Trial DetailsNCT Number: NCT06117176
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.
Interested in participating?
Request Info18 year and older
All sexes
Observational
Deutsches Herzzentrum der Charité and Charité, Berlin, Germany
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
Time frame: 30 days
Secondary study outcome parameters are the incidences of the major critical events and the number of incidents per case 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.
Contact information is provided by the study sponsor or research team.
Alexander Fuchs, MD
CONTACT
Thomas Riva, MD,PD
CONTACT
Insel Gruppe AG, University Hospital Bern
Other
Prospective Assessment Project of AirwaY Management-related Incidents in Adult Anaesthesia Care (PAPAYA III) - A European Multicentre Cross-sectional Observational Study
Acronym: PAPAYA-III
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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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