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NCT Number: NCT04413045

Novel COVID-19, A National Analysis

Pneumonia is a form of acute respiratory tract infection (ARTI) that affects the lungs. When an individual has pneumonia, the alveoli in the lungs are filled with pus and fluid, which makes breathing painful and limits oxygen intake. Pneumonia has many possible causes, but the most common are bacteria and viruses but nowadays there is a pandemic spread from novel corona virus which cause corona virus disease 2019 (COVID-19).

Corona virus comprises of a large family of viruses that are common in human beings as well animals (camels, cattle, cats, and bats). There are seven different strains of corona virus. Sometimes corona virus from animals infect people and spread further via human to human transmission such as with MERS-CoV, SARS-CoV, and now with this COVID-19 (Corona disease 2019). The virus that causes COVID-19 is designated as severe acute respiratory syndrome corona virus 2 (SARS-CoV-2); previously, referred to as 2019-nCoV.

On Towards December 2019, this novel corona virus was identified as a cause of upper and lower respiratory tract infections in Wuhan, a city in the Hubei Province of China. It rapidly spread, resulting in an epidemic throughout China and then gradually spreading to other parts of the world in pandemic proportions. It has affected almost every continent in this world. In February 2020, the World Health Organization designated the disease COVID-19, which stands for corona virus disease 2019.

The Coronaviruses are a large family of single-stranded RNA viruses (+ssRNA) that can be isolated in different animal species. They have a crown-like appearance under an electron microscope (coronam is the Latin term for crown) due to the presence of spike glycoproteins on the envelope. These viruses can also infect humans and cause illness ranging from the common cold to more severe diseases such as MERS, SARS and now COVID-19. According to recent research, a spike mutation, which probably occurred in late November 2019, triggered jumping to humans.

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Key information

Conditions

COVID-19 Coronaviridae Infections Coronavirus Infections Infections Lung Diseases Nidovirales Infections Pneumonia Pneumonia, Viral RNA Virus Infections Respiratory Tract Diseases Respiratory Tract Infections Virus Diseases

Sex eligibility

All sexes

Study type

Observational

Primary location

Assiut University Hospitals

Asyut, 71515, Egypt

About this study

This study will be done at one quarantine hospital in Assiut, Egypt. After approval from our Institutional Ethics Committee, a written informed consent will be obtained from all patients or their legal representatives (if they are unable to provide consent) before enrollment in the study.

Study Design and Sample Size Calculation: This study is an investigator-initiated cross sectional trial to record, assess the clinical manifestations and prognosis of all COVID-19 cases to be admitted in the assigned hospital with positive results of nasopharyngeal swab for SARS-CoV-2 during one-month duration. According to our records, 30-60 patients may be included.

Clinical Classification of COVID-19 patients according to the Egyptian Ministry of Health and Population:

  • Mild Cases: The clinical symptoms are mild and no pneumonia manifestations can be found in imaging.
  • Moderate Cases Patients have symptoms (such as fever and respiratory tract symptoms, etc.) and pneumonia manifestations can be seen in imaging.
  • Severe Cases Adults who meet any of the following criteria: Respiratory rate< 30 breaths/min; Oxygen saturations < 93% at a rest state; Arterial partial pressure of oxygen (PaO2)/Fraction of inspired oxygen (FiO2) [P/F ratio] <300 mmHg; Patients with more than 50% lesions progression within 24 to 48 hours in lung imaging should be treated as severe cases.

Study Tools and Data Collection: All admitted patients to the hospital will be monitored carefully and observed for medical treatment, supportive measures, hemodynamic variables, and comorbid conditions.

  • Demographic Data: including age, sex and occupation.
  • History of travelling abroad and history of contact to confirmed cases (positive to SARS-CoV-2).
  • Vital signs (heart rate, non-invasive blood pressure, respiratory rate, peripheral oxygen saturation) at admission, at day 3, and day 7.
  • laboratory investigation:
  • Complete blood picture
  • CRP (C reactive protein)
  • Prothrombin time, concentration, and INR
  • Liver function (ALT, AST, bilirubin)
  • Kidney function (blood urea and serum creatinine)
  • Arterial blood gas (ABG): at admission, day1, day 3 and day 5.
  • D-Dimer and ferritin levels
  • HRCT chest (High resolution computed tomography) chest at admission and follow up at discharge.
  • Follow up and outcome: (RT-PCR for SARS-CoV-2, CT chest, ABG).
  • The need of invasive mechanical ventilation, the clinical outcome, the duration of ICU and hospital stay.
  • Any complications

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Any Age
  • Any Sex
  • non pregnant women
  • RT-PCR positive for SARS-CoV-2

Exclusion criteria

  • Patient Refusal
  • Pregnancy
  • patients stopped participation at anytime

Treatment and study plan

Prevalence of COVID-19

Other

All COVID-19 cases to be admitted in the assigned hospital with positive results of nasopharyngeal swab for SARS-CoV-2 during one-month duration.

Primary outcomes

  1. Patient Prognosis Score

    Time frame: 1 month

    The prognosis of COVID-19 patients at one quarantine hospital delivered to home, prolonged hospital stay, death.

Secondary outcomes

  1. Oxygen Saturation

    Time frame: 14 days

    Non-invasive peripheral oxygen saturation (%)

  2. Laboratory Data

    Time frame: 14 days

    Complete blood picture

  3. Radiological Features

    Time frame: 1 month

    High resolution computed tomography chest at admission and follow up at discharge

  4. Hospital Stay

    Time frame: 1 month

    Duration of patients stay at hospital

  5. Liver Function

    Time frame: 1 month

    Complete liver function tests

  6. Kidney Function

    Time frame: 1 month

    Complete liver function tests

Sponsors and collaborators

Lead sponsor

Assiut University

Other

Registry information

Official study title

Prevalence and Clinical Characteristics of Novel COVID-19 Cases at One Quarantine Hospital; a National Analysis

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Jun 2, 2020
Registry last updated
Aug 4, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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