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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04455451
Other study ID # DCIR
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 6, 2020
Est. completion date September 30, 2021

Study information

Verified date September 2021
Source University Hospital Tuebingen
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Multi-center retrospective and prospective observational study of Covid-19 patients with severe or critical illness treated on a German ICU


Recruitment information / eligibility

Status Completed
Enrollment 2054
Est. completion date September 30, 2021
Est. primary completion date August 15, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age above 18 years - Covid-19 disease (positive SARS-CoV-2 PCR) Exclusion Criteria: -none

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Germany RWTH Aachen - Department for operative Intensive Care Medicine and intermediate Care Aachen
Germany Zollernalbklinikum Balingen
Germany Charité Universitätsmedizin Berlin Berlin
Germany UH Bochum - Department for Anesthesiology and Intensive Care Medicine Bochum
Germany Universitätsklinikum Bonn Bonn
Germany Universitätsklinikum Carl Gustav Carus Dresden Dresden
Germany Ev. Krankenhaus Bethesda Duisburg Klinik für Anästhesiologie und Intensivmedizin Duisburg
Germany Univerrsitätsklinikum Düsseldorf Düsseldorf
Germany Universitätsklinikum Essen Essen
Germany Universitätsklinikum Frankfurt Frankfurt
Germany University Hospital Freiburg - Department for Anesthesiology and Intensive Care Medicine Freiburg
Germany Universitätsklinikum Giessen Klinik für Anaesthesiologie und operative Intensivmedizin Gießen
Germany Universitätsmedizin Göttingen Klinik für Anästhesiologie Göttingen
Germany Universitätsklinikum Greifswald Greifswald
Germany Universitätsklinikum Halle Halle/Saale
Germany University Hospital Heidelberg - Department for Anesthesiologie and Intensive Care Medicine Heidelberg
Germany Universitätsklinikum des Saarlandes Homburg/Saar
Germany Klinikum der Universität Witten/Herdecke - Köln / Klinik für Anästhesiologie und operative Intensivmedizin Köln
Germany Universitätsklinikum Leipzig Leipzig
Germany UKSH Campus Lübeck - Department for Anesthesiology and Intensive Care Medicine Lübeck
Germany University Hospital Magdeburg - Department for Anesthesiology and Intensive Care Medicine Magdeburg
Germany Universitätsklinikum Marburg Marburg
Germany Technische Universität München München
Germany Oberschwabenklinik Ravensburg Klinik für Anästhesie-, Intensiv-, Notfall- und Schmerzmedizin Ravensburg
Germany University Hospital Tübingen - Department for Anesthesiology and Intensive Care Medicine Tübingen
Germany Universitätsklinikum Ulm Ulm
Germany Universitätsklinikum Würzburg Klinik und Poliklinik für Anästhesiologie, Intensivmedizin und Schmerztherapie Würzburg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital Tuebingen

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Mortality ICU Mortality of patients up to 150 days
Secondary ICU length of stay Intensive care unit length of stay up to 150 days
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