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临床试验/NCT04452942
NCT04452942Unknown不适用

Dynamic Changes in Cytokine and Eicosanoid Mediators Among Hospitalized Patients With Coronavirus Infectious Disease 2019 (COVID-19)

EicOsis Human Health Inc.1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2020年7月最近更新:
适应症

试验速览

阶段
不适用
入组人数
30
试验地点
1
主要终点
Changes on eicosanoid lipid mediators

研究概览

简要总结

This study is a prospective, single center, observational, cohort study of patients to (1) describe the kinetics and temporal relationship of changes in eicosanoid and cytokine mediators in patients with severe COVID-19 admitted to the hospital; and (2) correlate the dynamic changes in eicosanoid mediators with available patient clinical status, including measures of severity of illness, routine laboratory tests, and outcomes.

研究设计

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

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

  • Admitted to a hospital with symptoms suggestive of COVID-
  • Confirmed infection with SARS-CoV-2 as determined by polymerase chain reaction (PCR) or other commercial or public health assay in the 72 hours prior to hospital admission or any time during hospital admission.
  • Subject (or legally authorized representative) provides written informed consent prior to initiation of any study procedures.
  • Understands and agrees to comply with planned study procedures.
  • Agrees to the collection of whole blood samples.

排除标准

  • Inability to obtain informed consent.
  • Anticipated transfer to another hospital which is not a study site within 48 hours.
  • Inability to obtain sequential blood samples due to patient's characteristics (i.e. difficult vascular access).
  • Obstetric patients.

结局指标

主要结局

Changes on eicosanoid lipid mediators

时间窗: 10 days

Temporal changes on eicosanoid lipid mediators over a course of 10 days (or until discharge) in COVID-19 patients requiring hospitalization

Changes on plasma levels of a panel of 40 human cytokines and chemokines

时间窗: 10 days

Temporal changes on the levels of 40 human cytokines, chemokines and growth factors included in a commercially available panel (Bio-Rad, Human Chemokine Panel, 40-Plex #171AK99MR2) over a course of 10 days (or until discharge) in COVID-19 patients requiring hospitalization.

次要结局

  • Severe clinical outcome(Through study completion, an average of 10 days)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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