Skip to content

Ain Shams University Experience: Clinical Determinants of Hospitalized COVID-19 Patients

Ain Shams University Experience: Clinical Characteristics and Outcome Determinants of Hospitalized Covid-19 Patients at Ain Shams University Obour Hospital

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04584606
Enrollment
100
Registered
2020-10-14
Start date
2020-06-27
Completion date
2020-12-30
Last updated
2020-10-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronavirus Disease (COVID-19)

Brief summary

COVID-19 as a novel disease, different disease patterns were observed worldwide, and many treatment plans were tried. So, it is important to investigate the Egyptian clinical characteristics and different factors that determine the patient's 'outcome

Detailed description

Investigators will convey the Ain Shams University experience as the first university in Egypt to designate one of its hospitals (Ain Shams University Obour Hospital) for management of confirmed COVID19 cases. investigators will try to identify the characteristics of the disease as regards the clinical, laboratory and imaging abnormalities and to assess the outcome determinants. It is a retrospective observational cohort study at Ain Shams University Obour Hospital. All adult patients from both sexes with positive nucleic acid testing for severe adult respiratory syndrome Coronavirus (SARS-CoV-2)will be included. Clinical criteria, laboratory data, radiological findings, hospital course and patient outcome will be anonymously collected from records.

Interventions

DIAGNOSTIC_TESTLab workup (on admission and regularly during follow up).

Complete blood count with differential leucocytic count. Absolute lymphocytic and neutrophilic count. Liver functions: Aspartate transaminase and Alanine transaminase . Renal functions: Blood urea nitrogen, serum Creatinine. HbA1C. C-reactive protein (quantitative). Serum ferritin level. D - dimer level (quantitative). Coagulation profile (Prothrombin time/ Partial thromboplastin time/ International normalized ratio). Troponin level. Arterial blood gases when needed.

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult (≥18 years) patients from both sexes with positive nucleic acid testing for severe adult respiratory syndrome Coronavirus (SARS-CoV-2). * Standard of care arm of the ongoing clinical trials will be included in our study.

Exclusion criteria

* mild cases who don't need hospitalization

Design outcomes

Primary

MeasureTime frameDescription
RecoveryUntil patient is discharged or up to 12 weeks whichever comes firstRecovery defined as resolution of fever without the use of antipyretics, improvement of respiratory symptoms (e.g., cough, dyspnea) and no need for supplemental oxygen
MortalityUntil patient is discharged or up to 12 weeks whichever comes firstAll cause mortality

Secondary

MeasureTime frameDescription
Functional progression of the COVID 19 diseaseUntil patient is discharged or up to 12 weeks whichever comes firstincrease oxygen demands detected by arterial blood gases analysis and/or pulse oximeter
Conversion of nucleic acid testing for SARS-CoV-2 from positive to negative.Until patient is discharged or up to 12 weeks whichever comes firstDetected by Polymerase Chain Reaction (PCR) test for nasopharyngeal swab
Radiological progression of the COVID 19 diseaseUntil patient is discharged or up to 12 weeks whichever comes firstdetected by measuring the extent of pulmonary lesion in high resolution computed tomography (HRCT) of the chest

Countries

Egypt

Contacts

Primary ContactAshraf Elmaraghy
ashrafelmaraghy@yahoo.com+20 100 177 0703

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026