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临床试验/NCT05997485
NCT05997485撤回不适用

A Retrospective Observational Non-Interventional Study (NIS) to Assess Patient Characteristics Among COVID-19 Patients Receiving Treatment With Nirmatrelvir/Ritonavir (PAXLOVIDTM) in Morocco.

Pfizer0 个研究点开始时间: 2024年3月30日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
撤回
发起方
Pfizer
主要终点
Clinical Characteristics of Participants

研究概览

简要总结

The purpose of this study is to collect information on the:

  • general information of a group of people such as their age, sex, and other facts.
  • clinical information of the patients such as any other illness before having COVID 19.

In adult patients with COVID-19 who have been prescribed nirmatrelvir and ritonavir treatment.

This study will be conducted in Morocco. The study will capture information of the adult COVID-19 outpatients and inpatients who have been prescribed nirmatrelvir, ritonavir treatment. The inpatients will be admitted in the hospital for other reasons than COVID-19.

This study will have about 150 patients. The study will involve collection of patient information from medical records. The information collected can be either from papers or from computers.

The study will include patient information of those who:

  • are confirmed to have COVID-19 infection during the study period from 01 June 2022 to 30 June 2023.
  • are 18 years of age or older.
  • are prescribed Nirmatrelvir and ritonavir. This study will help to inform decision-making on use of Paxlovid at the national level.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Confirmed COVID-19 infection during the study period from 01 June 2022 to 30 June 2023
  • Nirmatrelvir, ritonavir written prescription

排除标准

  • There are no exclusion criteria for this study.

研究组 & 干预措施

Participants receiving Paxlovid Treatment

Patients administered oral Paxlovid as prescribed according to national Morocco treatment guidelines for Covid.

干预措施: Nirmatrelvir/Ritonavir (Drug)

结局指标

主要结局

Clinical Characteristics of Participants

时间窗: Approximately 01 June 2022 through 30 June 2023

Demographical Characteristics of Participants

时间窗: Approximately 01 June 2022 through 30 June 2023

Number of Participants with Pre-existing Comorbidities

时间窗: Approximately 01 June 2022 through 30 June 2023

次要结局

未报告次要终点

研究者

发起方
Pfizer
申办方类型
Industry
责任方
Sponsor

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