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Study on the efficacy of Xuanfeizhisou Mixture in the treatment of COVID-19 cough

Study on the efficacy of Xuanfeizhisou Mixture in the treatment of COVID-19 cough

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200006141
Enrollment
Unknown
Registered
2022-06-15
Start date
2022-06-01
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

COVID-19

Interventions

treatment group:usual care+Xuanfeizhisou Mixture
control group:usual care

Sponsors

Shuguang Hospital Affiliated to Shanghai University of T.C.M.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Patients with mild and moderate novel coronavirus pneumonia confirmed in accordance with the Diagnosis and Treatment Plan for Novel Coronavirus Pneumonia (Trial Version 9th); (2) TCM syndrome differentiation is wind evil and lung syndrome; (3) Two points for cough symptoms score; (4) Age is over 18-75 years old, with no limit on gender.

Exclusion criteria

Exclusion criteria: (1) Patients with severe pneumonia requiring mechanical ventilation and critical novel coronavirus pneumonia; (2) Those who are expected to die within 48 hours; (3) Respiratory tract infections caused by primary immune deficiency disease, acquired immune deficiency syndrome, congenital respiratory malformations, congenital heart disease, lung development abnormalities and other basic diseases; (4) Chest CT confirmed the existence of serious lung interstitial lesions and other underlying lung diseases; (5) According by the researchers, previous or current diseases may affect the outcome of patient trials or research, including malignant diseases, autoimmune diseases, severe malnutrition, etc.; and diseases that seriously affect the immune system, such as human immunodeficiency virus (HIV) infection, or blood system, or splenectomy, organ transplantation, etc. (6) Women during pregnancy and lactation.

Design outcomes

Primary

MeasureTime frame
cough index;

Secondary

MeasureTime frame
cough disappear rate at the 7th day;time of cough diappear day;TCM symdrome efficacy;cough VAS score;cough relieve time;

Countries

China

Contacts

Public ContactWei Zhang
zhangw1190a@sina.com13023153956

Outcome results

None listed

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