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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04775017
Other study ID # COVID-19-Delirium
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2021
Est. completion date December 2022

Study information

Verified date May 2022
Source Charite University, Berlin, Germany
Contact Claudia Spies, MD, Prof.
Phone +49 30 450 551102
Email claudia.spies@charite.de
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The global pandemic caused by the SARS-CoV-2 virus is confronting the German health system with a novel pathogen. This means that a timely evaluation of all available results is required. In the field of intensive care in particular, there are significant gaps in knowledge, particularly with regard to delirium. In this respect, this study also serves directly to investigate the pathways of delirium outcome in COVID-19 patients.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date December 2022
Est. primary completion date December 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: All patients with SARS-CoV-2 positive Covid-19 disease - Age=18 years - Proven by positive PCR tests from nasal/ throat swabs as well as samples from the deep respiratory tract. - Period 01.01.2020 to 21.02.2022 Exclusion Criteria: - NONE

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Germany Department of Anesthesiology and Operative Intensive Care Medicine Campus Virchow-Klinikum Berlin

Sponsors (1)

Lead Sponsor Collaborator
Charite University, Berlin, Germany

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of delirium Delirium is measured by validated screening scores. 01.01.2020 - 21.02.2022
Secondary Risk factors for severe COVID-19 Risk factors are defined according to actual literature e.g. obesity, diabetes or hypertension. 01.01.2020 - 21.02.2022
Secondary Patient characteristics Patient characteristics at hospital admission e.g. score level 01.01.2020 - 21.02.2022
Secondary Blood gas analysis Monitoring of blood gas analysis 01.01.2020-31.07.2020
Secondary Enteral nutrition Monitoring of enteral nutrition 01.01.2020-31.07.2020
Secondary Parenteral nutrition Monitoring of parenteral nutrition 01.01.2020 - 21.02.2022
Secondary Serum albumin Monitoring of serum albumin level 01.01.2020 - 21.02.2022
Secondary Total protein Monitoring of total protein level 01.01.2020 - 21.02.2022
Secondary Phosphate Monitoring of phosphate levels 01.01.2020 - 21.02.2022
Secondary Triglyceride Monitoring of triglyceride levels 01.01.2020 - 21.02.2022
Secondary Caloric intake Caloric intake is measured by total daily energy supply. 01.01.2020 - 21.02.2022
Secondary Respiratory setting Respiratory factors are measured respiratory setting 01.01.2020 - 21.02.2022
Secondary Inflammatory laboratory parameter 1 Monitoring of interleukine level 01.01.2020 - 21.02.2022
Secondary Inflammatory laboratory parameter 2 Monitoring of cytokine level 01.01.2020 - 21.02.2022
Secondary Inflammatory laboratory parameter 3 Monitoring of big immune status 01.01.2020 - 21.02.2022
Secondary Inflammatory laboratory parameter 4 Monitoring of t-cell population 01.01.2020 - 21.02.2022
Secondary Toxic-drug factors Toxic-drug factors are measured by concomitant medication. 01.01.2020 - 21.02.2022
Secondary Sociodemographic factors Sociodemographic factors are measured by Audit, Fagerström, occupation, age, gender, cognitive status. 01.01.2020 - 21.02.2022
Secondary Breathing hours Breathing hours are measured by non-invasive and invasive ventilation. 01.01.2020 - 21.02.2022
Secondary Length of intensive care unit stay Length of intensive care unit stay is measured in days of stay in the intensive care unit. 01.01.2020 - 21.02.2022
Secondary Length of hospital stay Length of hospital stay is measured in days of stay in hospital. 01.01.2020 - 31.07.2020
Secondary Adverse events Adverse Events defined by thromboembolic events, nosocomial infections, septic shock, acute renal failure, heart attack, post-intensive care syndrome and death are recorded until hospital discharge. 01.01.2020 - 21.02.2022
Secondary Post Intensive Care Unit Syndrome (PICS) Post Intensive Care Unit Syndrome (PICS) is measured by a validated battery (composite endpoint). 01.01.2020 - 21.02.2022
Secondary In-hospital mortality Mortality is measured in the hospital 01.01.2020 - 21.02.2022
Secondary Mortality Mortality is measured until 180 days 01.01.2020 - 21.02.2022
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