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To evaluate the clinical mechanism of Lian-Hua Qing-Wen capsule on systemic immune regulation of influenza patients

To evaluate the clinical mechanism of Lian-Hua Qing-Wen capsule on systemic immune regulation of influenza patients

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100054799
Enrollment
Unknown
Registered
2021-12-27
Start date
2022-01-06
Completion date
Unknown
Last updated
2022-12-05

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

Conditions

Influenza

Interventions

Sponsors

Ruijin Hospital, Shanghai Jiaotong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 69 Years

Inclusion criteria

Inclusion criteria: 1. Meet the clinical diagnostic criteria for influenza in the "Influenza Diagnosis and Treatment Program (2020 Edition)"; 2. Aged 18 to 70 years; 3. Fever duration =38.5 degree; 4. Throat swab is positive for influenza virus rapid antigen test; 5. Sign the informed consent form, and the informed consent process complies with the regulations; 6. Influenza patients who have been injected with new crown vaccine patients for more than 1 month.

Exclusion criteria

Exclusion criteria: 1. Severe or critical cases of influenza, or diagnosed as pharyngeal conjunctival fever, herpetic angina, suppurative tonsillitis, etc.; 2. Those taking Xiyanping, Reduning, Tanreqing, Jinhuaqinggan, Banlangen and other traditional Chinese medicine preparations and/or immunomodulators with antiviral effects, or external use of drugs with immunomodulatory effects within 1 week before the selection; 3. Suffering from diseases that seriously affect the immune system, such as: human immunodeficiency virus (HIV) infection, or blood system, or splenectomy, organ transplantation, etc.; 4. Complications of influenza such as sinusitis, otitis media, bronchitis and pneumonia have occurred; 5. Antiviral drugs have been used within 48 hours before the visit; 6. Systemically receiving steroid therapy or other immunosuppressive therapy; 7. Have a history of epilepsy or febrile convulsions; 8. Patients with severe malnutrition, rickets and serious primary diseases of the heart, brain, liver, kidney and hematopoietic system; 9. Allergic to known components of the test drug; 10. According to the judgment of the researcher, other diseases or conditions that reduce the possibility of enrollment or complicate enrollment, such as unstable living environment, inconvenient transportation, etc., are likely to cause loss to follow-up.

Design outcomes

Primary

MeasureTime frame
Immune cell genus;Inflammatory factors;

Countries

China

Contacts

Public ContactYe Jing

Ruijin Hospital

carlionje8@126.com+86 18121263409

Outcome results

None listed

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