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A Real-world Retrospective Study of Disease Outcomes in Non-severe COVID-19 Patient

S

Shanghai Vinnerna Biosciences

Status

Enrolling

Conditions

COVID-19 Patient

Study type

Observational

Funder types

Industry

Identifiers

NCT05489874
JT001-013-COVID-19

Details and patient eligibility

About

Retrospective analysis of real-world disease outcomes in non-severe COVID-19 patients with high risk factors of progression to severe disease, including death, without definitive anti-SARS-CoV-2 treatment

Full description

This is a retrospective, observational, real-world study to review outcomes of Mild to Moderate COVID-19 patients admitted to Ruijin Hospital Affiliated to Shanghai Jiaotong University School of Medicine (hereinafter referred to as Ruijin Hospital) from March to June 2022. These patients should be with risk factors for progression to severe disease (including death) and without definitive anti-novel coronavirus (SARS-CoV-2) treatment. The database of this study will be the hospital information system (HIS) of Ruijin Hospital.

Enrollment

2,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age ≥18 years old;

  2. A record of positive SARS-CoV-2 nucleic acid test results on the day of admission or on the second day;

  3. Diagnosed as mild or common novel coronavirus pneumonia on admission, or with at least one of the following COVID-19-related symptoms on admission: fever, cough, sore throat, nasal congestion or runny nose, headache, muscle pain, nausea, vomiting, diarrhea , shortness of breath or difficulty breathing, chills or chills;

  4. Documented or diagnosed high risk factors for progression to severe COVID-19 (including death) with one or more of the following:

    • Age ≥ 60 years
    • Cardiovascular disease (including congenital heart disease) or high blood pressure
    • Chronic lung disease (eg chronic obstructive pulmonary disease [COPD], asthma [moderate to severe], interstitial lung disease, cystic fibrosis and pulmonary hypertension)
    • diabetes
    • Has an immunosuppressive disorder or is receiving immunosuppressive therapy (eg, long-term use of corticosteroids or other immunosuppressive drugs leading to decreased immune function)
    • Obese or overweight (BMI>25 kg/m2)
    • Sickle cell disease
    • Active cancer
    • Chronic kidney disease
    • Current smokers
    • Neurodevelopmental disorders (eg, cerebral palsy, Down syndrome) or other conditions that cause medical complexity (eg, genetic or metabolic syndrome and severe congenital anomalies)
    • Need for relevant medical support (not related to COVID-19) (eg tracheostomy, gastrostomy or positive pressure ventilation, etc.)

Exclusion criteria

  1. Diagnosed with severe/critical COVID-19 before or on the day of admission;

  2. There is a data record of having received the following treatments before progression to severe/critical COVID-19:

    • Nematicavir/ritonavir combination package (ie Paxlovid)
    • SARS-CoV-2 monoclonal antibody (Ambavirumab/Romisevirumab)
    • Convalescent COVID-19 plasma
    • Other anti-SARS-CoV-2 drugs under investigation

Trial contacts and locations

1

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Central trial contact

Yali Pan, Project Directer; Jie Wang, Project Manager

Data sourced from clinicaltrials.gov

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