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The efficacy of lianhuaqingwen in the treatment of patients infected with novel coronavirus variant Omicron

The efficacy of lianhuaqingwen in the treatment of patients infected with novel coronavirus variant Omicron

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200057841
Enrollment
Unknown
Registered
2022-03-19
Start date
2022-03-18
Completion date
Unknown
Last updated
2023-11-13

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

Lianhuaqingwen treatment group:6g/time, 3 times a day

Sponsors

The First Affiliated Hospital of Shandong First Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients infected with the Omicron variant; 2. Patients with mild or moderate clinical symptoms; 3. Patients vaccinated with novel Coronavirus vaccine; 4. Patients who can voluntarily sign written informed consent forms.

Exclusion criteria

Exclusion criteria: 1. Patients on antiviral or antibiotic drugs; 2. Chronic respiratory disease, respiratory bacterial infection and other respiratory diseases affecting the study; 3. Patients with serious primary diseases of heart, brain, lung, liver, kidney and hematopoietic systems, as well as mental diseases; 4. Patients with anaphylaxis to Lianhuaqingwen;

Design outcomes

Primary

MeasureTime frame
Rate of disappearance of symptoms on day 14;

Secondary

MeasureTime frame
The time of the nucleic acid test turns negative;Time of disappearance of antibody IgM;Absorption time of chest CT lesions;

Countries

China

Contacts

Public ContactXuedong Liu/Liang Dong

The First Affiliated Hospital of Shandong First Medical University

2946229207@qq.com+86 0531-89269215

Outcome results

None listed

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