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临床试验/NCT04335188
NCT04335188已完成不适用

COVID-19 Registry Rhineland-Palatinate (Germany) - COVID-19 Disease Registry a National, Multicentre, Non-interventional, Prospective Observational Study

IHF GmbH - Institut für Herzinfarktforschung1 个研究点 分布在 1 个国家目标入组 2,589 人开始时间: 2020年4月6日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
2,589
试验地点
1
主要终点
Chest x-ray

研究概览

简要总结

Documentation of all patients undergoing inpatient treatment for SARS-CoV-2 infection with regard to clinical status at admission, medical history, inpatient treatment and course of disease. The aim is to create a risk stratification of the infection on the basis of clinical data as well as therapy and disease progression of the patients. This may also contribute to a better planning of resources.

研究设计

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

入排标准

性别
All
接受健康志愿者

入选标准

  • In-patients fulfilling the following criteria:
  • SARS-CoV-2 infection In-patient treatment Written informed consent for participation in observational study

排除标准

  • No explicit medical exclusion criteria are stated to avoid selection bias.

结局指标

主要结局

Chest x-ray

时间窗: throughout study completion, in average 1.5 years

presence of infiltrates

Medication

时间窗: throughout study completion, in average 1.5 years

number of patients with medication changes

Chest CT

时间窗: throughout study completion, in average 1.5 years

presence of infiltrates

Supportive care - ICU

时间窗: throughout study completion, in average 1.5 years

number of patients with ICU treatment required

Intra-hospital complications

时间窗: throughout study completion, in average 1.5 years

number of patients with complications during hospital stay

Therapeutic strategies

时间窗: throughout study completion, in average 1.5 years

number of patients with ECMO required

Supportive care - oxygen therapy

时间窗: throughout study completion, in average 1.5 years

number of patients with oxygen therapy required

Supportive care - ventilation

时间窗: throughout study completion, in average 1.5 years

number of patients with ventilation required

Lab parameters

时间窗: throughout study completion, in average 1.5 years

number of patients with significant changes in lab parameters

Vital status at discharge

时间窗: throughout study completion, in average 1.5 years

vital status at discharge: alive, dead

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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