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

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

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05778318
Enrollment
200
Registered
2023-03-21
Start date
2023-03-20
Completion date
2024-06-30
Last updated
2023-05-11

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

Conditions

COVID-19 Pneumonia

Brief 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.

Interventions

DRUGThe 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.

OTHERThe group of patients who did not receive Lianhua Qingwen orally

The group of patients who did not receive Lianhua Qingwen orally.

Sponsors

Qianfoshan Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* For patients infected with the Omicron variant, the diagnostic criteria are confirmed cases of COVID-19 and clinical classification according to the diagnostic criteria of Prevention and Control Protocol for COVID-19 (Trial Eighth Edition) issued by the National Health and Construction Commission. * The clinical symptoms were classified as mild or ordinary. * They have been vaccinated against the COVID-19.

Exclusion criteria

* Patients receiving antiviral or antibiotic drugs * Severe and critical patients with COVID-19. * Patients with chronic respiratory diseases, bacterial infections of the respiratory system, and other respiratory diseases affecting the study. * Patients with serious primary diseases of the heart, brain, lung, liver, kidney, and hematopoietic systems, as well as mental diseases. * Allergic reaction to Lianhua Qingwen granules. * Excluded patients treated with the same drug as Lianhua Qingwen.

Design outcomes

Primary

MeasureTime frameDescription
Disappearance rate of symptomstwo weeksDisappearance rate of symptoms (fever, fatigue, cough)

Countries

China

Contacts

Primary ContactQian Qi, Dr.
qiqianqlh@163.com+86 13706380314

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026