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Research on traditional Chinese medicine preparation of clearing heat and detoxifying to treat epidemic disease and reduce the conversion from mild to severe (Anti-epidemic Special No.: 2022009).

Research on traditional Chinese medicine preparation of clearing heat and detoxifying to treat epidemic disease and reduce the conversion from mild to severe

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200005801
Enrollment
Unknown
Registered
2022-04-03
Start date
2022-04-01
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-2019

Interventions

The intervention group:a combination of conventional therapy and traditional chinese medicine treatment

Sponsors

Shenzhen Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) The mild and ordinary patients who meet the diagnostic criteria of COVID-19; (2) 70 years old = 14 years old; (3) did not receive other clinical studies before selection; (4) voluntarily accepted the trial and signed the informed consent form.

Exclusion criteria

Exclusion criteria: (1) pregnant and lactating women; (2) patients with delirium, dementia and various psychosis; (3) patients with chronic respiratory diseases, including chronic bronchitis, bronchial asthma, chronic obstructive pulmonary disease, bronchiectasis, pulmonary fibrosis, pulmonary tuberculosis (uncured) and so on. (4) patients with autoimmune-related diseases (psoriasis, ankylosing spondylitis, etc.) were treated with biological agents in the past month. (5) patients with known experimental drug allergy (6) patients with heart, liver and renal insufficiency before selection; (7) patients with malignant tumor, blood system disease or immune deficiency; (8) patients who were treated with glucocorticoid for a long time; (9) patients with other diseases before selection were determined to interfere with the results of clinical trials.

Design outcomes

Primary

MeasureTime frame
Nucleic acid detection negative time;The percentage of subjects who changed from mild to severe;a clinical symptom score;

Secondary

MeasureTime frame
Laboratory indicators;Length of hospital stay;Chest imaging changes;

Countries

Chinese

Contacts

Public ContactLiu yuxiang
gsjlyx111@163.com13688806425

Outcome results

None listed

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