Trials / Unknown
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
| Type | Name | Description |
|---|---|---|
| DRUG | The group of patients who received Lianhua Qingwen orally | Lianhua 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. |
| OTHER | The group of patients who did not receive Lianhua Qingwen orally | The 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.