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Study for efficacy and safety of Jie-Xing-Jun-Zi granules in the Treatment of convalescent patients of novel coronavious pneumonia (COVID-19)

Study for efficacy and safety of Jie-Xing-Jun-Zi granules in the Treatment of convalescent patients of novel coronavious pneumonia (COVID-19)

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000032313
Enrollment
Unknown
Registered
2020-04-25
Start date
2020-05-01
Completion date
Unknown
Last updated
2020-04-27

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

Beijing University of Chinese Medicine Third Affiliated Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Convalescent patients with novel coronavious pneumonia,and the patient is aged 18-75 years old; (2) The TCM syndrome type conforms to deficiency of 'qi' and 'yin' and not exhausted of 'Yu Xie'; (3) Voluntary test, or the immediate family or the client's approved client agrees to the test, and voluntarily signs the informed consent; (4) Provide detailed contact information, no short-term willingness to move and be willing to cooperate with followers.

Exclusion criteria

Exclusion criteria: (1) Patients with fasting water due to gastrointestinal bleeding, intestinal obstruction, etc; (2) Patients with pre-existing severe brain, heart, liver, kidney and hematopoietic system diseases; (3) Patients who are known to be allergic to the ingredients of the intervention drug; (4) Patients who are unable to cooperate with follow-up.

Design outcomes

Primary

MeasureTime frame
TCM syndrome curative effect;

Secondary

MeasureTime frame
Quality of Life;6MWD;Lung function;Chest CT examination;Reversion rate of viral nucleic acid;

Countries

China

Contacts

Public ContactHongsheng Cui

Beijing University of Chinese Medicine, Third Affiliated Hospital

hshcui@sina.com+86 13901101359

Outcome results

None listed

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