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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05158816
Other study ID # f/2021/097
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 8, 2021
Est. completion date November 30, 2022

Study information

Verified date December 2022
Source Jessa Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Retrospective single center analyses of COVID-19 patients admitted to the ICU between 01/02/2020 and 31/07/2021.


Description:

All adults (>18 years) with acute hypoxaemic respiratory failure due to diagnosed COVID-19 pneumonia and admitted to ICU from 01/02/2020 until 31/07/2021 were included in the study. Following the World Health Organisation (WHO) protocol 19, laboratory confirmation of COVID-19 infection was defined as a positive result on polymerase chain reaction (PCR) assays of nasopharyngeal swab samples or bronchoalveolar lavage. Only laboratory-confirmed patients were included in the analysis. Additional data collection Additional collected parameters are listed below and are collected as a standard-of-care in our hospital: - Demographics: i.e age, gender, BMI - DNR code - Comorbidities: smoking, obesity, hypertension, diabetes, cardiovascular disease, respiratory disease, malignancies, renal failure (AKI), liver failure, gastrointestinal disease, neurological conditions, mental state, other - Symptoms at the time of admission to ICU: i.e fever, body temperature, dyspnoea, headache, diarrhea etc… - Laboratory results of all standard parameters measured - Treatment: antiviral agents, antibiotics, etc… - Complications: shock, heart failure, sepsis, stroke, etc… - Ventilation: method, PEEP, FiO2, P/F ratio ..


Recruitment information / eligibility

Status Completed
Enrollment 295
Est. completion date November 30, 2022
Est. primary completion date November 30, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - All adult COVID-19 patients (>18 years) admitted to the ICU between 01/02/2020 and 31/07/2021 with a laboratory confirmation of COVID-19 infection with a positive result on polymerase chain reaction (PCR) assays of nasopharyngeal swab samples or bronchoalveolar lavage Exclusion Criteria: - All adult patients admitted for other reasons to the ICU (no COVID-19 pneumonia)

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
ECMO
Patients undergoing extracorporeal membrane oxygenation

Locations

Country Name City State
Belgium Jessa Hospital Hasselt Limburg

Sponsors (1)

Lead Sponsor Collaborator
Jessa Hospital

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Other Complications description of possible complications after ECMO through study completion, an average of 1 year
Primary Mortality mortality of patients during their stay at the ICU through study completion, an average of 1 year
Secondary 3 Months Mortality Mortality of patients 3 months after admission to ICU
Secondary acute kidney injury incidence of acute kidney injury through study completion, an average of 1 year
Secondary continous renal replacement therapy incidence of continous renal replacement therapy through study completion, an average of 1 year
Secondary Length of stay in hospital Length of stay in hospital through study completion, an average of 1 year
Secondary Length of stay in ICU Length of stay in ICU during ICU stay
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