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A Randomized Controlled Trial for Qingyi No. 4 Compound in the treatment of Convalescence Patients of Novel Coronavirus Pneumonia (COVID-19)

A Randomized Controlled Trial for Qingyi No. 4 Compound in the treatment of Convalescence Patients of Novel Coronavirus Pneumonia (COVID-19)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000029947
Enrollment
Unknown
Registered
2020-02-16
Start date
2020-03-01
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

Sponsors

Longhua Hospital Affiliated to Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria forconfirmed cases in the Diagnosis and Treatment of Pneumonia of New Coronavirus Pneumonia (Trial Version 5); 2. The acute stage is complicated by sepsis, respiratory failure, ARDS and so on. The patients are with multiple organ damage when improved and tended to recover after organ support and other treatments; 3. Meet the TCM diagnostic criteria for the recovery period; 4. Aged 18-75 years-old men or women; 5. Patients who volunteer to participate in this study and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with respiratory failure, acute necrotizing encephalopathy, septic shock, multiple organ dysfunction, and other serious clinical conditions requiring monitoring and treatment when enrolled; 2. Pregnant, preparing or lactating women; 3. Patients with severe heart, cerebrovascular and liver, kidney, hematopoietic system diseases and mental illness; 4. Patients with tuberculosis, measles, AIDS and other infectious diseases; 5. Patients with known allergies to western medicine or traditional Chinese medicine ingredients used in this research; 6. Patients with gastrointestinal bleeding who cannot take Chinese medicine; 7. Patients who use oral Chinese medicine within 4 weeks.

Design outcomes

Primary

MeasureTime frame
Lung function;

Secondary

MeasureTime frame
Total duration of disease;Time needed for healing;Incidence of adverse events;Number of sequelae;SF-36;Mental health scale;

Countries

China

Contacts

Public ContactLU Zhenhui

Longhua Hospital Affiliated to Shanghai University of Traditional Chinese Medicine

tcmdoctorlu@163.com+86 13817729859

Outcome results

None listed

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