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CLINICAL_TRIALS ClinicalTrials.gov record update

Implementation of Routine Recording of Intraoperative Adverse Events According to ClassIntra® During the Sign-out Phase of the WHO Surgical Safety Checklist Using a Multifaceted, Tailored Implementation Strategy: Protocol of a Collaborative Before- and After-cohort Project

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT05818332
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-25T22:26:51.804974+00:00
Published At
2025-02-11T00:00:00+00:00
Record Updated At
2025-02-11
Timestamp Basis
source retrieval time was not retained by the feed adapter
Date limitation
source retrieval time was not retained by the feed adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions
["Perioperative Patient Safety"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2025-02-11"
protocolSection.identificationModule.nctId
"NCT05818332"
protocolSection.identificationModule.officialTitle
"Implementation of Routine Recording of Intraoperative Adverse Events According to ClassIntra\u00ae During the Sign-out Phase of the WHO Surgical Safety Checklist Using a Multifaceted, Tailored Implementation Strategy: Protocol of a Collaborative Before- and After-cohort Project"
protocolSection.statusModule.overallStatus
"RECRUITING"
protocolSection.designModule.phases
[]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Perioperative Patient Safety (protocolSection.conditionsModule.conditions)

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

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