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A randomized, open and controlled clinical trial for traditional Chinese medicine in the treatment of novel coronavirus pneumonia (COVID-19)

A randomized, open and controlled clinical trial for traditional Chinese medicine in the treatment of novel coronavirus pneumonia (COVID-19)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000029855
Enrollment
Unknown
Registered
2020-02-15
Start date
2020-02-15
Completion date
Unknown
Last updated
2020-02-17

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

Chinese traditional medicine group 1:Traditional Chinese medicine qingfei prescription treatment
Chinese traditional medicine group 2:Traditional Chinese medicine clear lung prescription and compound houttuynia mixture treatment
Control group:Conventional treatment

Sponsors

The First Affiliated Hospital of Medical College of Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) common type pneumonia patients with confirmed new coronavirus infection; 2) aged 18 to 75 years old; 3) voluntary signing of written informed consent.

Exclusion criteria

Exclusion criteria: 1) pneumonia patients with severe or critical new coronavirus infection; 2) daily treatment of asthma, any other chronic respiratory disease; 3) patients with confirmed history of diabetes and HbA1C >=8.0%; 4) those allergic to the known ingredients of the drug; 5) pregnant or nursing women; 6) patients with severe mental illness; 7) patients who have participated in other clinical trials within the past 1 month.

Design outcomes

Primary

MeasureTime frame
TCM symptom score;Antifebrile time;The time and rate of transition of new coronavirus to Yin;

Countries

China

Contacts

Public ContactWu Guolin

The First Affiliated Hospital of Medical College of Zhejiang University

wuguolin28@163.com+86 13136150848

Outcome results

None listed

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