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临床试验/NCT04466306
NCT04466306已完成不适用

SARS-CoV2 Pediatric Acute Kidney Injury Registry and Collaborative

Children's Healthcare of Atlanta47 个研究点 分布在 7 个国家目标入组 400 人开始时间: 2020年4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
400
试验地点
47
主要终点
Acute Kidney Injury (AKI)

研究概览

简要总结

This study is an observational registry of children with or suspected to have SARS CoV2 (COVID-19) admitted to pediatric intensive care units (PICU). This registry will help describe the prevalence, rate and severity of acute kidney injury (AKI) in children with Severe Acute Respiratory Syndrome Coronavirus-2(SARS CoV2) across the world. The registry will be developed using a point prevalence methodology and then full retrospective review. Once a week, from April through June 2020, data collection will occur in "real-time" to estimate a weekly point prevalence of AKI and renal replacement therapy (RRT). The operational definition of "patients under investigation" (PUIs) will be used to identify the denominator of patients to be studied. The PUIs will be cohorted into SARS CoV2 test positive, test negative, test pending, or test unavailable. The primary aim of this study is to deliver a global, objective data driven analysis of the burden of AKI in virus positive patients or patients under investigation (PUI) who are admitted to the pediatric intensive care unit.

详细描述

The primary purpose of the data collection will be to provide a descriptive analysis of the burden and characteristics of AKI in children with SARS-CoV2 proven or suspected infection across the world. This is a prospective, point prevalence study. Data collection will occur once a week during the months of April through June 2020.

The protocol for the point prevalence is for each individual participating site to conduct a surveillance study on predetermined dates of their intensive care units (pediatric medical, surgical, cardiac ICUs) for patients by the inclusion and exclusion criteria. The study is strictly observational. Data will only be captured on the predetermined dates listed. The dates have been chosen to reflect the estimated surge and peak of the virus spread in North America, Europe, Africa, Asia, and Australia. The rationale for performing an urgent point prevalence estimation study first, includes the following: a) there is almost no knowledge on AKI rate, severity of AKI or how current pandemic-setting AKI phenotype differs from what we know of AKI in children prior to the pandemic. A rapidly-performed, high feasibility-designed point prevalence estimation study, with minimal data collection will provide rapid, almost instantaneous dissemination of results to the international community. Based on the results of this study, a follow-up study is planned for a full retrospective data collection of all viral positive patients. Understanding the burden of pediatric AKI during this pandemic within the current context of acute health burden in the healthcare settings and enable planning and feasibility evaluation for quality of care measures and potentially for upcoming technology needs and/or sharing of RRT technology with adult care units; b) an urgent point-prevalence estimation study with minimal but key data collection will inform on any changes to design, sample size requirements or data points for the larger granular longitudinal retrospective study.

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
7 Days 至 25 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Patient less than or equal to 25 years of age
  • Receiving clinical care in the pediatric intensive care unit (PICU) on a study day in April - June 2020
  • Patient considered a "Person Under Investigation" and/or tested positive for SARS-CoV2 (COVID-19)

排除标准

  • 未提供

结局指标

主要结局

Acute Kidney Injury (AKI)

时间窗: 14 days

Kidney Disease Improving Global Outcomes (KDIGO) Staged AKI by serum creatinine or urine output

次要结局

  • Fluid overload(Day of Enrollment)
  • Survival(14 days)
  • Rate of nephrotoxic medication exposure(Day of Enrollment)
  • Rate of Extracorporeal Therapy Requirement(14 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (47)

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