- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02513537
Postoperative Delirium - European Society of Anaesthesiology Survey
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
Conditions
Study Type
Enrollment (Actual)
Contacts and Locations
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
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Anaesthesists, nursing staff, which are invited to the online - Survey of the European Society of Anaesthesiology
Study Plan
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
Investigators
- Study Director: Claudia Spies, MD, Prof., Charité - Univeristy Medicine Berlin
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PODESAS
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
-
Sengkang General HospitalRecruitingDelirium and Post-operative Cognitive Dysfunction (POCD) | Delirium, Postoperative | Delirium - PostoperativeSingapore
-
Wonkwang University HospitalCompleted
-
Nanjing First Hospital, Nanjing Medical UniversityActive, not recruitingPostoperative Delirium (POD)China
-
Qin ZhangNational Natural Science Foundation of ChinaRecruiting
-
Qin ZhangNational Natural Science Foundation of ChinaRecruitingDelirium, PostoperativeChina
-
Hao LiCompleted
-
Chinese PLA General HospitalXiangya Hospital of Central South University; The Affiliated Nanjing Drum Tower... and other collaboratorsCompletedPostoperative Delirium (POD)China
-
Riverside University Health System Medical CenterNot yet recruitingPostoperative Delirium (POD) | Norepinephrine | Ephedrine
-
University Hospital, Basel, SwitzerlandInnosuisse - Swiss Innovation AgencyCompletedPostoperative Delirium (POD)Switzerland
-
Qianfoshan HospitalNot yet recruitingOpioid-Free Anaesthesia | Delirium - PostoperativeChina