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Critical Incident During Anaesthesia

Critical Incident During Anaesthesia

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05435287
Enrollment
92
Registered
2022-06-28
Start date
2021-08-01
Completion date
2021-12-31
Last updated
2022-06-28

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

Conditions

Critical Incident, Safety Issues

Keywords

patient safety, critical incident, anaesthesia

Brief summary

A multicenter study in Ukrainian hospitals on compliance with the requirements for responding to critical cases in the operating room, and the availability of relevant documentation and checklists.

Detailed description

Timely information and response to emergencies are important both in the context of patient safety and in the context of the hospital economy. The availability of information systems is one of the security requirements of the Helsinki Declaration of Patient Safety. Ukraine has only just begun its path to implementing the Declaration of Helsinki in Ukrainian hospitals. The level of adherence to the recommendations can vary considerably depending on the region, the provision of the hospital and the effectiveness of the institution's internal management. In our survey of Ukrainian hospitals, only 74% of hospitals kept records of anaesthesia complications in general, with only 46% having separate electronic or paper documents to record complications; Also, the majority of respondent physicians (62.9%) reported the absence of checklists or algorithms for actions in case of emergencies or emergencies during anaesthesia.

Interventions

None listed

Sponsors

Bogomolets National Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* critical incident during anaesthesia: massive hemorrhage \>1000ml, difficult intubation, severe hypotension, severe bradycardia, desaturation, cardiac arrest, high spinal block, anesthetic toxicity, miocardial ischemia, severe arhytmia etc

Exclusion criteria

* critical incidents without aneasthesia

Design outcomes

Primary

MeasureTime frameDescription
Critical Incident During Anaesthesia5 monthsCritical Incident During Anaesthesia

Secondary

MeasureTime frameDescription
The use of the WHO Safe Surgery checklist5 monthsThe use of the WHO Safe Surgery checklist
Keeping records of the critical incidents5 monthsKeeping records of the critical incidents during anaesthesia

Countries

Ukraine

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026