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Randomized, controlled clinical study on efficacy and safety of yibing jiedu decoction in treating mild and common novel coronavirus pneumonia

Randomized, controlled clinical study on efficacy and safety of yibing jiedu decoction in treating mild and common novel coronavirus pneumonia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200067183
Enrollment
Unknown
Registered
2022-12-28
Start date
2022-12-25
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

COVID-19

Interventions

control arm:symptomatic treatment
trial arm:symptomatic treatment + Disease detoxification decoction

Sponsors

Cangzhou Hospital of Integrated Traditional Chinese and Western Medicine, Hebei
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1 Subjects tested positive for novel coronavirus nucleic acid or antigen ; 2 according to the current version of the ' new coronavirus pneumonia diagnosis and treatment program ', the clinical classification was mild or common type ; 3 Age = 18 years old ; 4 Subjects were able to follow all visiting arrangements, treatment plans, laboratory tests and other research procedures, and voluntarily signed written informed consent.

Exclusion criteria

Exclusion criteria: 1 Aphasia or other patients who could not cooperate to complete the scale evaluation ; 2 Patients who were receiving COVID-19 monoclonal antibody, convalescent plasma, or other prohibited combined drugs within 28 days before screening ; 3 have a history of adverse reactions to known Chinese medicine ingredients ; 4 severe lung disease before onset ; 5 Patients who participated in clinical trials of other drugs within 4 weeks before screening ; 6. Screening patients who had used drugs with pharmacological or clinical effects against the novel coronavirus or traditional Chinese medicine containing components similar to the test drugs within 7 days before the examination, including but not limited to Jinhua Qinggan, Lianhua Qingwen, Banlangen, Azvudine ; 7 patients with immunodeficiency ( such as : malignant tumors, AIDS patients, organ or bone marrow transplants, long-term use of corticosteroids or other immunosuppressive drugs causing immune dysfunction ) ; 8 Suspected or had a history of alcohol, drug abuse or mental illness ; 9 any history of gastrointestinal diseases affecting drug absorption ( including but not limited to reflux esophagitis, chronic diarrhea, inflammatory bowel disease, intestinal tuberculosis, gastrinoma, short bowel syndrome, subtotal gastrectomy, etc. ) ; 10 chronic kidney disease ( including chronic kidney disease stage 3-5 ), chronic liver disease ( such as liver fibrosis, cirrhosis, or serum AST and / or ALT = 3 times the upper limit of normal ; pregnant or lactating women ; the researchers believed that other patients were not suitable for this study.

Design outcomes

Primary

MeasureTime frame
Median time and 7 d negative conversion rate of novel coronavirus nucleic acid;

Secondary

MeasureTime frame
Main TCM symptom score;Disappearance time of fever symptoms;Incidence of COVID-19 related severe and critical illness;

Countries

China

Contacts

Public Contactwang lixin

Cangzhou Hospital of Integrated Traditional Chinese and Western Medicine, Hebei

azai2010@126.com13343379856

Outcome results

None listed

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