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UnknownNCT05778318

Efficacy of Lianhua Qingwen in Treating Patients Infected With the Omicron Variant of the COVID-19

Status
Unknown
Phase
Study type
Observational
Enrollment
200 (estimated)
Sponsor
Qianfoshan Hospital · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

A retrospective analysis was conducted on patients infected with the Omicron variant of COVID-19 diagnosed from August 2022 to now. Patients were divided into observation groups and control groups according to whether or not oral Lianhua Qingwen granules were used. Through data analysis and follow-up, the effectiveness of Lianhua Qingwen in treating patients infected with the Omicron variant of COVID-19 was discussed.

Conditions

Interventions

TypeNameDescription
DRUGThe group of patients who received Lianhua Qingwen orallyLianhua Qingwen Granules: oral. One bag at a time, three times a day. The course of treatment for mild and ordinary cases of novel coronavirus pneumonia is 7-10 days.
OTHERThe group of patients who did not receive Lianhua Qingwen orallyThe group of patients who did not receive Lianhua Qingwen orally.

Timeline

Start date
2023-03-20
Primary completion
2024-04-30
Completion
2024-06-30
First posted
2023-03-21
Last updated
2023-05-11

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05778318. Inclusion in this directory is not an endorsement.

Efficacy of Lianhua Qingwen in Treating Patients Infected With the Omicron Variant of the COVID-19 (NCT05778318) · Clinical Trials Directory