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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04817397
Other study ID # ICU admitted COVID-19 patients
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 20, 2021
Est. completion date August 30, 2021

Study information

Verified date October 2021
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

1. ry outcome includes the correlation between lymphocyre /neurtophll ratio (LNR) and mortality rate during hospital stay in the ICU admitted COVID 19 patients. 2. ry outcome(s) include the LNR and its correlation with ICU stay, the need for mechanical ventilation, renal impairment.


Description:

In December 2019,the COVID-19 virus has been mainly breaking out in Wuhan in China as pneumonia affecting patients . Common clinical features During hospitalization started to appear including acute respiratory infection , inflammatory reaction , fever, pneumonia, cough, fatigue , anosmia . The patient known suspected if he has a clinical picture of viral pneumonia, exposure history, and radiographic findings [CT] or [MRI] chest consistent with COVID-19 pneumonia. the gold standard and the Final diagnosis (PCR) positivity for the presence of coronavirus . The immune response to respiratory infection causes neutrophils to collect inside the lung especially the alveoli. Neutrophils aggregation may lead to collateral tissue damage and cytotoxicity. According to Previous studies apoptosis of lymphocytes occurred due to the release of anti-inflammatory cytokines resulting in lymphopenia. high levels of circulating neutrophils have been demonstrated in COVID-19 patients( A lot of literatures and studies have demonstrated the value of what is called neutrophil/ lymphocyte ratio (LNR) as a simple prognostic ratio correlated to morbidity and mortality. Up to our knowledge, there is no study utilized such ratio in COVID-19 ICU admitted patients, so that, this study has been built


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date August 30, 2021
Est. primary completion date July 30, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Adult patients (aged =18 years) 2. Patients who need non-invasive ventilation (NIV or CPAP) or invasive ventilation (intubation) Exclusion Criteria: 1. Previous diagnosis of severe liver or kidney failure. 2. Patients with Human Immunodeficiency Virus (HIV) infection. 3. Patients with previous hematological diseases (Leukemia) that condition alterations in blood counts. 4. Consumption of treatments with any type of immunosuppressants prior to admission that conditions low lymphocytes. 5. Patients with bone marrow depression.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Egypt Assuit University Assiut

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary The Lymphocyte/neutrophil ratio The Lymphocyte/neutrophil ratio as a prognostic index for short term outcome in the ICU admitted COVID-19 adult patients up to 30 days
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