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临床试验/NCT05996770
NCT05996770尚未招募不适用

Evaluation of the Safety and Efficacy of Azvudine and Paxlovid in the Treatment of Hospitalized Patients With COVID-19

Xiao Li,MD0 个研究点目标入组 1,500 人开始时间: 2024年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
1,500
主要终点
mortality

研究概览

简要总结

In this retrospective study, we aimed to evaluate the clinical efficacy and safety of two antiviral drugs on COVID-19 and inpatients with existing complications in the First Affiliated Hospital of Shandong First Medical University. In addition, we also explored a key issue. Is the combined treatment effect of two antiviral drugs, Paxlovid and Azvudine, better than the use of a single drug?

详细描述

We conducted a single center retrospective cohort study on hospitalized patients with severe acute respiratory syndrome coronavirus type 2 infection who received treatment with nimatevir/ritonavir tablets or azivudine tablets at the First Affiliated Hospital of Shandong First Medical University from December 1,2022 to January 31,2023. In the research of this project, it is necessary to extract, sort out and retrospectively analyze the clinical data of all patients with COVID-19 who have received Nematovir/Ritonavir tablets or Azivudine tablets in the First Affiliated Hospital of Shandong First Medical University (Shandong Qianfoshan Hospital), and respectively identify the relevant epidemiological characteristics of COVID-19 patients, It is planned to use multiple linear regression or logical regression model to explore the relevant factors that affect the drug use efficiency index, safety index and total cost of patients with COVID-19, so as to provide scientific and quantitative evidence support for the drug use mode of the disease, the clinical value of the drug and the rational drug use of patients, and also provide favorable basis for the supervision and decision-making of smart pharmacy of medical institutions.

研究设计

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

入排标准

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

入选标准

  • The patient's admission time is from December 1,2022 to January 31,
  • The patient has used either Paxlovid or azivudine tablets during admission.
  • Age ≥ 18 years old. Exclusion Criteria:
  • Patients using other antiviral drugs.
  • Patients with incomplete clinical data.

排除标准

  • 未提供

结局指标

主要结局

mortality

时间窗: Through study completion,up to half a year.

Mortality rate of patients with COVID-19 treated with COVID-19 Medicine

次要结局

未报告次要终点

研究者

发起方
Xiao Li,MD
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Xiao Li,MD

Associate professor of pharmacy

Qianfoshan Hospital

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