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A prospective, multicenter registry-based, cross-sectional study: Epidemiology of adverse events attributed to extubation in paediatric anaesthesia

A prospective, multicenter, registry-based, cross-sectional study to elucidate risk factors for extubation-related adverse events in pediatric anesthesia - Extubation in Pediatric Anesthesia Study: ExPEDIA

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1030250100
Enrollment
8500
Registered
2025-05-14
Start date
2025-10-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Extubation-related adverse outcome PRAE,CEs

Interventions

None listed

Sponsors

Okuyama Megumi
Lead Sponsor
Kojima Taiki
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: All of the following 1. Patients under 18 years of age who have undergone general anesthesia and are scheduled for extubation 2. Cases in the operating room and outside the operating room (CT/MRI quality, radiotherapy room, catheterization room, general ward) 3. First enrolled cases at each study site during the study period

Exclusion criteria

Exclusion criteria: If any of the following applies 1. Non-intubated cases (airway securing with supraglottic devices is not excluded) 2. Patients with a tracheostomy 3. Patients scheduled for postoperative intubation management (patients who were not scheduled to be extubated at the time of the start of general anesthesia) 4. Cases in which the family or the patient refuses to participate in the study, regardless of the reason 5. Duplicate cases

Design outcomes

Primary

MeasureTime frame
Critical respiratory complications following extubation

Secondary

MeasureTime frame
(1) total complications after extubation (2) SpO2 drop values before and after extubation, SpO2 10% or greater drop in SpO2

Contacts

Public ContactMegumi Okuyama

Institute of Science Tokyo Hospital

okuyama.megumi@tmd.ac.jp+81-3-3813-6111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026