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Clinical trial of Huashi Baidu granule for treatment of COVID-19 in children

A randomized, controlled, single-center clinical observational trial of the effectiveness and safety of Huashi Baidu granules in the treatment of children with mild COVID-19 infection

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059732
Enrollment
Unknown
Registered
2022-05-10
Start date
2022-05-01
Completion date
Unknown
Last updated
2024-03-25

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

Conditions

COVID-19

Interventions

control group:Regular treatment

Sponsors

Shanghai Children‘s Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1. Patients with mild Covid-19 infection aged 3-18 years old (in line with the diagnostic criteria of the Diagnosis and Treatment Program for Novel Coronavirus Pneumonia (Trial Ninth Edition)); Covid-19 nucleic acid PCR test is positive, regardless of sex; 2. With symptoms of cough and expectoration; 3. The course of disease is within 5 days; 4. Have not used traditional Chinese medicine or Chinese patent medicine preparations with similar functions to this prescription within 24 hours before joining the group; 5. Agree to sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. It is not guaranteed to take medicine during the observation period of this study; 2. Those who have major basic diseases, or chronic basic diseases in the acute stage, or need long-term oral or injection drugs; 3. History of severe allergic reactions to ingredients in Huashi Baidu granule; 4. Taking other Chinese patent medicines or traditional Chinese medicines during the screening period and research period; 5. Participants in other COVID-19 related clinical trials; 6. Patients and guardians are unable to cooperate to complete the study and follow-up.

Design outcomes

Primary

MeasureTime frame
Negative time of nucleic acid;

Secondary

MeasureTime frame
Improvement of TCM symptoms and signs;

Countries

China

Contacts

Public ContactGao Jian

Shanghai Children‘s Medical Center

gaojian@scmc.com.cn+86 18918320295

Outcome results

None listed

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