COVID-19 and Liver Injury in Patients With or Without Underlying Liver Disease: A Multi-centre Retrospective-prospective Observational Study
COVID-19 and liver injury in patients with or without underlying liver disease: A multi-centre retrospective-prospective observational study.
All patients infected with SARS-CoV-2 and admitted to the COVID-19 ward/ICU of Max Hospital Saket (either in East Wing , Max Super Specialty Hospital, Saket or MAX Smart Super Specialty Hospital, Saket) between 1/4/2020 to 30/6/2020 (retrospective data between 1/4/2020- 30/5/2020 & prospective data from approval till 30/6/2020), will be included
研究概览
地位
条件
详细说明
COVID-19 and liver injury in patients with or without underlying liver disease: A multi-centre retrospective-prospective observational study.
All patients infected with SARS-CoV-2 and admitted to the COVID-19 ward/ICU of Max Hospital Saket (either in East Wing , Max Super Specialty Hospital, Saket or MAX Smart Super Specialty Hospital, Saket) between 1/4/2020 to 30/6/2020 (retrospective data between 1/4/2020- 30/5/2020 & prospective data from approval till 30/6/2020), will be included Primary objectives
- To study the prevalence of liver live injury & factors associated with among patients in-fected with SARS-CoV-2.
- To study the prevalence of new liver injury and factors associated with it, among patient with underlying liver disease who develops COVD-19.
Secondary objectives
- To correlate the presence and degree of liver dysfunction with the clinical outcomes in these patients.
- To define the incidence of development of acute liver failure among these patients
研究类型
注册 (预期的)
联系人和位置
学习地点
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Dlelhi
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New Delhi、Dlelhi、印度、110017
- Max Super Speciality hospital, Saket (A unit of Devki Devi Foundation)
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
取样方法
研究人群
描述
Inclusion Criteria:All patients infected with SARS-CoV-2 and admitted to the COVID-19 ward/ICU of Max Hospital Saket (either in East Wing , Max Super Specialty Hospital, Saket or MAX Smart Super Specialty Hospital, Saket) between 1/4/2020 to 30/6/2020 (retrospective data between 1/4/2020- 30/5/2020 & prospective data from approval till 30/6/2020), will be included.
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Exclusion Criteria:
- Patients less that 18 years old with COVID-19
- Pregnant ladies with COVD-19
- Unwilling to give consent for inclusion
学习计划
研究是如何设计的？
设计细节
- 观测模型：队列
- 时间观点：其他
研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
COVID-19 Positive Case
大体时间：4-8 weeks
|
To study the prevalence of liver live injury & factors associated with among patients in-fected with SARS-CoV-2.
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4-8 weeks
|
|
COVID-19 Positive Case
大体时间：4-8 weeks
|
To study the prevalence of new liver injury and factors associated with it, among patient with underlying liver disease who develops COVID-19.
|
4-8 weeks
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
COVID-19 Positive Case
大体时间：4-8 weeks
|
To correlate the presence and degree of liver dysfunction with the clinical outcomes in these patients.
|
4-8 weeks
|
|
COVID-19 Positive Case
大体时间：4-8 weeks
|
To define the incidence of development of acute liver failure among these patients
|
4-8 weeks
|
合作者和调查者
调查人员
- 首席研究员：Kaushal Madan, DM、max healthcare
研究记录日期
研究主要日期
学习开始 (预期的)
初级完成 (预期的)
研究完成 (预期的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- COVID 19/LI/2020
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)？
IPD 计划说明
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
在美国制造并从美国出口的产品
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