跳至主要内容
临床试验/NCT05778318
NCT05778318招募中不适用

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

Qianfoshan Hospital1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2023年3月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
200
试验地点
1
主要终点
Disappearance rate of symptoms

研究概览

简要总结

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.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

  • Patients receiving antiviral or antibiotic drugs
  • Severe and critical patients with COVID-
  • 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.

研究组 & 干预措施

Control group

Patients without Lianhua Qingwen treatment.

干预措施: The group of patients who did not receive Lianhua Qingwen orally (Other)

Observation Group

Patients with Lianhua Qingwen treatment.

干预措施: The group of patients who received Lianhua Qingwen orally (Drug)

结局指标

主要结局

Disappearance rate of symptoms

时间窗: two weeks

Disappearance rate of symptoms (fever, fatigue, cough)

次要结局

未报告次要终点

研究者

发起方
Qianfoshan Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Qian Qi

Dr.

Qianfoshan Hospital

研究点 (1)

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