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APRICOT: Anaesthesia PRactice In Children Observational Trial

NCT01878760 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30000

Last updated 2015-10-14

No results posted yet for this study

Summary

The aims of the APRICOT study are:

* To establish the incidence of severe critical events in children undergoing anesthesia in Europe.
* To describe the differences in paediatric anaesthesia practice throughout Europe.
* To study the potential impact of this variability on the occurrence of severe critical events (Laryngospasm, Bronchospasm, Pulmonary aspiration, Drug error, Anaphylaxis, Cardiovascular instability, Neurological damage, Perianaesthetic cardiac arrest and postanaesthetic Stridor).

Conditions

  • Anaesthesia
  • Children

Sponsors & Collaborators

  • European Society of Anaesthesiology

    lead OTHER

Principal Investigators

  • Walid Habre, M.D. · University Hospital, Geneva

  • Francis Veyckemans, M.D. · Cliniques Universitaires St Luc asbl Brussels

Eligibility

Max Age
15 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-03-31
Primary Completion
2015-01-31
Completion
2015-04-30

Countries

  • Austria
  • Belgium
  • Croatia
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Gibraltar
  • Greece
  • Ireland
  • Israel
  • Italy
  • Kosovo
  • Latvia
  • Lithuania
  • Malta
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Russia
  • Serbia
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • Switzerland
  • Turkey (Türkiye)
  • Ukraine
  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01878760 on ClinicalTrials.gov