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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02513537
Other study ID # PODESAS
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 2015
Est. completion date December 2020

Study information

Verified date June 2019
Source Charite University, Berlin, Germany
Contact Claudia Spies, MD, Prof.
Phone +49 30 450 55 10 01
Email claudia.spies@charite.de
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Recruiting
Enrollment 400
Est. completion date December 2020
Est. primary completion date December 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

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

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Germany Department of Anaesthesiolgy and Intensive Care Medicine CVK/CCM, Charité - Univeristy Medicine Berlin Berlin
Italy Italian National Research Centres On Aging Ancona
Italy Department of Anaesthesiology, Critical Care and Pain Medicine, Sapienza "University of Rome" Rome
Spain Department of Anaesthesiology, Faculdad de medicina de Valladloid, Hospital Universitario Rio Hortega Valladolid
United Kingdom Department of Anaesthesia, Imperial College NHS Healthcare Trust London

Sponsors (1)

Lead Sponsor Collaborator
Charite University, Berlin, Germany

Countries where clinical trial is conducted

Germany,  Italy,  Spain,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Status of diagnosis of delirium 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
Primary Status of prevention of delirium 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
Primary Status of therapy of delirium 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 Status of diagnosis of delirium 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
Secondary Status of prevention of delirium 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
Secondary Status of therapy of delirium 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
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