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临床试验/NCT04570488
NCT04570488已完成不适用

Predicting Favorable Outcomes in Hospitalized Covid-19 Patients

NYU Langone Health1 个研究点 分布在 1 个国家目标入组 1,415 人开始时间: 2020年5月15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
1,415
试验地点
1
主要终点
Reduction in days from first low-risk score to discharge

研究概览

简要总结

Testing use of predictive analytics to predict which COVID-19+ patients are at low risk for an adverse event (ICU transfer, intubation, mortality, hospice discharge, re-presentation to the ED, oxygen requirements exceeding nasal cannula at 6L/Min) in the next 96 hours

详细描述

To assess if display of low risk of adverse event in EPIC can safely reduce length of stay and plan for discharge.

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 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult hospitalized COVID19+ patients predicted to have no adverse event at 96 events with a threshold at 90% PPV, with at least one low risk during their admission who are discharged alive and have not been in the ICU

排除标准

  • Age < 18 years not hospitalized for COVID19+.

结局指标

主要结局

Reduction in days from first low-risk score to discharge

时间窗: 96 Hours

Reduction in days from first low-risk score to discharge

次要结局

  • Reduction in length of stay (LOS)(96 hours)
  • Reduction in GTD vs. LOS(96 hours)
  • No change in 30 day re-ED presentation or hospital admission rate for cohort(96 hours)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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