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Clinical study on the treatment of influenza and upper respiratory tract infection (febrile virus attack lung syndrome) with Qingfeidayuan granules

Clinical study on the treatment of influenza and upper respiratory tract infection (febrile virus attack lung syndrome) with Qingfeidayuan granules

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2100005151
Enrollment
Unknown
Registered
2021-08-08
Start date
2021-08-09
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

Upper respiratory infection

Interventions

Control group:Qingfei Dayuan granule simulant
Experimental group:Qingfei Dayuan particles

Sponsors

Hubei Provincial Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Meet the clinical diagnostic criteria for influenza or the diagnostic criteria for acute upper respiratory tract infection; 2. Comply with the standard of TCM heat-toxin attacking the lung syndrome; 3. Aged 18-70 years; 4. Fever duration =37.3?; 5. The informed consent process complies with the regulations, and the informed consent form is signed.

Exclusion criteria

Exclusion criteria: 1. Severe or critical cases of influenza, or diagnosed as novel coronavirus pneumonia, pharyngeal conjunctival fever, herpetic angina, suppurative tonsillitis, etc.; 2. Complications of influenza such as sinusitis, otitis media and pneumonia have occurred; 3. The anti-influenza virus drugs included in the ''Influenza Diagnosis and Treatment Program (2020 Edition)'' have been used within 48 hours before the visit; 4. Systemically receiving steroid therapy or other immunosuppressive therapy; 5. Have a history of epilepsy or febrile convulsions; 6. Patients with severe malnutrition, rickets and serious primary diseases of the heart, brain, liver, kidney and hematopoietic system; 7. Pregnant or breastfeeding patients, allergic constitution, allergic to multiple drugs or allergic to known components of the research drug; 8. According to the judgment of the investigator, 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
Time for complete reduction of fever;

Secondary

MeasureTime frame
Incidence of complications and weight loss;Rate of disappearance of individual symptoms and time required for disappearance or remission;TCM syndrome effect;Viral antigen negative conversion rate;Blood routine examination;

Countries

China

Contacts

Public ContactBa Yuanming
1723426138@QQ.COM+86 13871013338

Outcome results

None listed

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