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Efficacy and Safety of Corticosteroids in COVID-19

Not Applicable
Completed
Conditions
Novel Coronavirus Pneumonia
COVID-19
Interventions
Registration Number
NCT04273321
Lead Sponsor
Beijing Chao Yang Hospital
Brief Summary

There is still controversy about the effective of glucocorticoids for the treatment of novel coronavirus pneumonia. This is a prospective randomized controlled trails. The aim is to explore the effectiveness and safety of glucocorticoids in the treatment of novel coronavirus pneumonia.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
86
Inclusion Criteria
  • age more than 18 years old
  • accord with the clinical diagnosis and/ or etiological diagnosis diagnostic criteria of Novel coronavirus pneumonia (COVID-19).
  • admitted in the general wards
  • be able to sign informed consent
Exclusion Criteria
  • severe immunosuppression (HIV infection, long-term use of immunosuppressive agents
  • pregnant or lactation period women
  • glucocorticoids are needed for other diseases
  • unwilling or unable to participate or complete the study
  • participate in other study

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
MP groupMethylprednisolone-
Primary Outcome Measures
NameTimeMethod
the incidence of treatment failure in 14 days14 days

The clinical symptoms and signs continue to deteriorate, or new pulmonary or extrapulmonary lesions appear, or the chest imaging indicates the progress, and the patient is transferred to ICU or intubation and invasive ventilation or died.

Secondary Outcome Measures
NameTimeMethod
the duration of virus change to negative30 days

the duration from admission to virus negative

mortality at day 3030 days

the patient die in 30 days

ICU admission rate in 30 days30 days

the patients transform to ICU because of clinical deteriorate in 30 days

clinical cure incidence in 14 days14 days

The clinical symptoms and signs improved or alleviated (the temperature be normal , respiratory symptoms improved significantly, imaging showed obvious absorption) and no additional or alternative treatment was needed.

Trial Locations

Locations (7)

Beijing YouAn Hospital

πŸ‡¨πŸ‡³

Beijing, China

the first peopel hospital of Xiangyang

πŸ‡¨πŸ‡³

Xiangyang, China

Tianyou Hospital Affiliated to Wuhan University of science and technology

πŸ‡¨πŸ‡³

Wuhan, China

Yichang first people's Hospital

πŸ‡¨πŸ‡³

Yichang, Hubei, China

Hubei province hospital of integrated Chinese & Western Medicine

πŸ‡¨πŸ‡³

Wuhan, Hubei, China

Renmin Hospital of Wuhan University

πŸ‡¨πŸ‡³

Wuhan, China

Union Hospital Affiliated to Tongji Medical College of Huazhong University of science and technology

πŸ‡¨πŸ‡³

Wuhan, China

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