Postoperative Delirium - European Society of Anaesthesiology Survey

February 10, 2025 updated by: Claudia Spies, Charite University, Berlin, Germany

The ESA is currently preparing a guideline on the management of postoperative delirium (POD), which attempts to reduce the impact of postoperative delirium and provide recommendations for prevention, diagnostics and treatment of delirium outside the intensive care unit. The guidelines are going to be published during 2015.

While the guideline provides recommendations for daily practice, assessment of current practice and knowledge is of utmost importance, because the implementation and the measurement of a change in clinical practice will be dependent on these measurements.

This Survey has been approved by the Scientific and Research Committees of the European Society of Anaesthesiology (ESA), the Media Committee of the ESA, as well as the institutional ethical committee of Charité - Universitätsmedizin Berlin.

Study Overview

Status

Completed

Study Type

Observational

Enrollment (Actual)

564

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Berlin, Germany, 13355
        • Department of Anaesthesiolgy and Intensive Care Medicine CVK/CCM, Charité - Univeristy Medicine Berlin
      • Ancona, Italy, 60127
        • Italian National Research Centres On Aging
      • Valladolid, Spain, 47012
        • Department of Anaesthesiology, Faculdad de medicina de Valladloid, Hospital Universitario Rio Hortega
      • London, United Kingdom, SW7 2 AZ
        • Department of Anaesthesia, Imperial College NHS Healthcare Trust

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

Anaesthesists , nursing statt and students (Members of the European Society of Anaesthesiology)

Description

Inclusion Criteria:

  • Anaesthesists, nursing staff, which are invited to the online - Survey of the European Society of Anaesthesiology

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Status of diagnosis of delirium
Time Frame: Up to 6 months
Answers of ESA-members regarding diagnosis instruments of Delirium. Survey: Multiple Chioce Question. Plus short Essay question to describe prevention (non-structured, non mandatory).
Up to 6 months
Status of prevention of delirium
Time Frame: Up to 6 months
Answers of ESA-members regarding prevention measurements of Delirium Survey: Multiple Chioce Question. Plus short Essay question to describe prevention (non-structured, non mandatory).
Up to 6 months
Status of therapy of delirium
Time Frame: Up to 6 months
Answers of ESA-members regarding therapy of Delirium. Survey: Multiple Chioce Question. Plus short Essay question to describe prevention (non-structured, non-mandatory).
Up to 6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Status of diagnosis of delirium
Time Frame: Up to one, two and five years
Answers of ESA-members regarding diagnosis instruments of Delirium. Survey: Multiple Chioce Question. Plus short Essay question to describe prevention (non-structured, non-mandatory).
Up to one, two and five years
Status of prevention of delirium
Time Frame: Up to one, two and five years
Answers of ESA-members regarding prevention measurements of Delirium. Survey: Multiple Chioce Question. Plus short Essay question to describe prevention (non-structured, non-mandatory).
Up to one, two and five years
Status of therapy of delirium
Time Frame: Up to one, two and five years
Answers of ESA-members regarding therapy of Delirium. Survey: Multiple Chioce Question. Plus short Essay question to describe prevention (non-structured, non-mandatory).
Up to one, two and five years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Claudia Spies, MD, Prof., Charité - Univeristy Medicine Berlin

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

August 1, 2015

Primary Completion (Actual)

December 1, 2020

Study Completion (Actual)

December 1, 2020

Study Registration Dates

First Submitted

March 20, 2015

First Submitted That Met QC Criteria

July 30, 2015

First Posted (Estimated)

July 31, 2015

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 10, 2025

Last Verified

February 1, 2025

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Postoperative Delirium

Subscribe