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

A Real-world Retrospective Study of Disease Outcomes in Non-severe Coronavirus Disease 2019 (COVID-19) Patients With Risk Factors for Severe COVID-19

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05489874
Enrollment
2000
Registered
2022-08-05
Start date
2022-07-14
Completion date
2024-12-30
Last updated
2022-08-05

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

Conditions

COVID-19 Patient

Brief summary

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

Detailed 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.

Interventions

None listed

Sponsors

Shanghai Vinnerna Biosciences Co., Ltd.
Lead SponsorINDUSTRY

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

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

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

Design outcomes

Primary

MeasureTime frameDescription
Percentage of patients with COVID-19 progressionup to 3 monthsPercentage of patients with COVID-19 progression (defined as progression to severe/critical COVID-19 or death from any cause).

Secondary

MeasureTime frameDescription
SARS-CoV-2up to 3 monthsTime from first SARS-CoV-2 positive to continuous negative
SARS-CoV-2 continuous negativeup to 3 monthsTime from admission to SARS-CoV-2 continuous negative
SARS-CoV-2 Ct valuesup to 3 monthsChanges in SARS-CoV-2 Ct values
Percentage of participantsup to 3 monthsPercentage of participants who experience these events * Progress to severe COVID-19 * Progress to critical COVID-19 * Death from any cause * Admission to ICU * Mechanical Ventilation * Progress to severe COVID-19 * Progress to critical COVID-19 * Death from any cause * Admission to ICU * Mechanical Ventilation
Length of hospital stayup to 3 monthsLength of hospital stay related to COVID-19
safetyup to 3 monthsAbnormal results of vital signs (respiration)beats per minute
chest CT scanup to 3 monthsChanges in chest CT scan

Countries

China

Contacts

Primary ContactJie Wang, Project Manager
jie_wang5@junshipharma.com8618036618073
Backup ContactYali Pan, Project Directer
yali_pan@junshipharma.com8618621590299

Outcome results

None listed

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