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Chinese medicine prevention and treatment program for novel coronavirus pneumonia (COVID-19): a perspective, double-blind, placebo, randomised controlled trial

A prospective randomized double-blind placebo-controlled study of traditional Chinese medicine staging regimen in the treatment of novel coronavirus pneumonia (COVID-19)

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2000002964
Enrollment
Unknown
Registered
2020-02-03
Start date
2020-02-04
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

novel coronavirus pneumonia (NCP)

Interventions

Sponsors

Zhejiang Chinese Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Patients who meet the diagnostic criteria of the common type of confirmed cases (the initial stage of clinical treatment of traditional Chinese medicine) or the severe cases of confirmed cases (the middle stage of clinical treatment of traditional Chinese medicine); (2) The cases of common type (the initial stage of clinical treatment of traditional Chinese medicine) belong to the type of cold-dampness stagnant lung; (3) The confirmed cases were severe (in the middle stage of clinical treatment of traditional Chinese medicine). (4) The patients knew and agreed to participate in this study.

Exclusion criteria

Exclusion criteria: (1) The critically ill patients in the diagnosis and treatment program of pneumonia with new coronavirus infection issued by the National Health Commission; (2) It is not suitable for patients who take traditional Chinese medicine decoction; (3) Those with other serious organ diseases or mental diseases; (4) Those who are allergic to or have contraindications to the drugs involved in the study scheme.

Design outcomes

Primary

MeasureTime frame
Recovery time;Ratio and time of severe progression to critical or even death;Ratio and time for the general type to progress to heavy;

Secondary

MeasureTime frame
Relief of clinical symptoms (fever, fatigue, gastrointestinal discomfort, etc.) and duration;Average length of hospital stay;Quality of life (SF 36);Lung HRCT score improvement;Adverse event rate;Improvement of TCM syndromes;

Countries

China

Contacts

Public ContactWen Chengping

Zhejiang Chinese Medical University

wengcp@163.com+86 13906514781

Outcome results

None listed

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