European Surgical Outcomes Study

NCT01203605 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 46985

Last updated 2012-09-05

No results posted yet for this study

Summary

The European Surgical Outcomes Study (EuSOS) is a multi-centre, international cohort study of peri-operative care and clinical outcomes for patients undergoing non-cardiac surgery.

Participating centres throughout Europe will contribute routine clinical data describing all eligible patients who undergo surgery from 4th April 2011 to 11th April 2011. Patients will then be followed until hospital discharge (or for a maximum of 60 days) for duration of hospital stay and hospital mortality. Routine clinical data will also be collected for those patients admitted to critical care at any stage after surgery but during the same hospital admission. Specific objectives are to describe clinical outcomes and standards of peri-operative care for patients undergoing non-cardiac surgery in Europe.

Conditions

  • Non-cardiac Surgery

Sponsors & Collaborators

  • European Society of Anaesthesiology

    collaborator OTHER
  • European Society of Intensive Care Medicine

    collaborator OTHER
  • Queen Mary University of London

    lead OTHER

Principal Investigators

  • Rupert Pearse, MBBS FRCA MD · Queen Mary's University of London, UK

  • Andrew Rhodes, MBBS FRCA · St Georges Hospital, London UK

  • Rui Moreno, MD · Hospital de Santo António dos Capuchos, Lisboa, Portugal

  • Paolo Pelosi, MD · University of Insubria, Varese, Italy.

  • Claudia Spies, MD · Charite University, Berlin, Germany

  • Jean-Louis Vincent, MD PhD · Erasme Hospital, Free University of Brussels, Belgium.

  • Benoit Vallet, MD PhD · Centre Hospitalier Universitaire de Lille, France.

  • Philip Metnitz, MD · Medizinische Universität Wien, Austria.

  • Peter Bauer, PhD · Medizinische Universität Wien, Austria.

  • Andreas Hoeft, MD PhD · University Hospital Bonn, Germany

Eligibility

Min Age
16 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-04-30
Primary Completion
2011-06-30
Completion
2011-06-30

Countries

  • Belgium
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Iceland
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Serbia
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • Switzerland
  • 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 NCT01203605 on ClinicalTrials.gov