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Xuanfei Baidu granules for mild and ordinary type of COVID-19: a retrospective study

Xuanfei Baidu granules for mild and ordinary type of COVID-19: a retrospective study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200059819
Enrollment
Unknown
Registered
2022-05-12
Start date
2022-07-10
Completion date
Unknown
Last updated
2024-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Corona Virus Disease 2019

Interventions

Observation group:Xuanfei Baidu granules
Control group:Conventional therapy

Sponsors

Tianjin University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Mild/ordinary COVID-19 patients. The diagnosis criteria were referred to COVID-19 Diagnosis and Treatment Protocol (Trial Version 9).

Exclusion criteria

Exclusion criteria: 1. Accompanied by serious underlying diseases affecting survival, including uncontrolled and clinically significant heart, kidney, digestive, blood diseases, neuropsychiatric diseases, immune diseases, metabolic diseases, malignant tumors, severe malnutrition, etc.; 2. Allergic constitution, allergic to the drug components involved in the treatment plan; 3. pregnant or lactating women; 4. Unable to cooperate in mental state, suffering from mental diseases, having no self-control and unable to express themselves clearly; 5. Participating in other clinical trials; 6. According to the judgment of the investigator, there will be patients whose efficacy and safety evaluation will be affected by complications of enrollment or poor compliance.

Design outcomes

Primary

MeasureTime frame
Time of virus nucleic acid test turning negative;The hospitalization time;

Secondary

MeasureTime frame
Symptom resolution rate;

Countries

China

Contacts

Public ContactZhuang Junhua

Tianjin University of Traditional Chinese Medicine

zjhtcm@foxmail.com+86 13902020873

Outcome results

None listed

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