Skip to content

A randomized, open, parallel-controlled clinical trial on the efficacy and safety of Jingyebaidu granules in treating novel coronavirus pneumonia (COVID-19)

A randomized, open, parallel-controlled clinical trial on the efficacy and safety of Jingyebaidu granules in treating novel coronavirus pneumonia (COVID-19)

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2000002999
Enrollment
Unknown
Registered
2020-02-12
Start date
2020-02-15
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

novel coronavirus pneumonia (COVID-19)

Interventions

Sponsors

Tongji Hospital, Tongji Medical College of HUST
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients who were confirmed diagnosis of 2019-ncov virus pneumonia, according to the "pneumonia diagnosis and treatment program for novel coronavirus infection (trial version 5)",including clinical symptoms, pulmonary CT manifestations and positive nucleic acid test; 2. Inpatients 18 years old (including 18), regardless of gender; 3. Willing to participate in this clinical trial and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with severe pneumonia requiring mechanical ventilation and severe new coronavirus infection with pneumonia; 2. Death is expected within 48 hours; 3. There is clear evidence of bacterial infection in respiratory tract infections caused by primary immunodeficiency disease, acquired immunodeficiency syndrome, congenital respiratory tract malformation, congenital heart disease, gastroesophageal reflux disease, pulmonary dysplasia and other basic diseases; 4 subjects with the following conditions: daily treatment of asthma, any other chronic respiratory diseases, respiratory bacterial infections such as suppurative tonsillitis, acute tracheal bronchitis, sinusitis, otitis media and other respiratory diseases that affect clinical trial evaluation.Chest CT confirmed the existence of severe pulmonary interstitial lesions, bronchiectasis and other basic pulmonary diseases; 5. According to the researcher's judgment, the previous or current diseases may affect the patient's participation in the trial or the outcome of the study, including malignant diseases, autoimmune diseases, severe malnutrition, liver and kidney diseases, blood diseases, nervous system diseases, and endocrine diseases;He is suffering from serious diseases that affect the immune system, such as human immunodeficiency virus (HIV) infection, or blood system, or splenectomy, organ transplantation, etc. Unable to cooperate in mental state, suffering from mental disease, unable to control, unable to express clearly; Allergic constitution (such as allergic to two or more drugs or food) or history of allergy to this product and conventional treatment drugs; 8. A history of substance abuse or dependence; 9. Pregnant or nursing women; 10. Other researchers consider it inappropriate to participate in clinical trials.

Design outcomes

Primary

MeasureTime frame
Validity observation index;

Secondary

MeasureTime frame
Safety observation index;

Countries

China

Contacts

Public ContactLiu Dong

Institutional Review Board, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology

ld_2069@163.com+86 13507183749

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026