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