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临床试验/NCT06685367
NCT06685367招募中不适用

The Cost-effectiveness of Artificial Intelligence Acute Kidney Injury Prediction Auxiliary Software (Acura AKI)

Huede Healthtech Co., Ltd.1 个研究点 分布在 1 个国家目标入组 3,600 人开始时间: 2024年10月17日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
3,600
试验地点
1
主要终点
Acute kidney injury (AKI) incidence

研究概览

简要总结

"Huede" AI Aided AKI Prediction Software, Acura AKI, uses machine learning algorithms to predict the risk of AKI within the next 24 hours and provide a ranking of feature importance. By using Acura AKI, physicians can assess the risk of AKI, focusing on high-risk patients to provide care decisions. This study will be conducted in a prospective randomized clinical trial in adult ICUs, implementing the Acura AKI system for predicting AKI. The study aims to determine whether early prediction and intervention using the Acura AKI system can improve the outcomes of critically ill patients with adverse kidney conditions. The study endpoint is to evaluate the cost-effectiveness of using Acura AKI, including the incidence of AKI, dialysis rates, mortality rates, length of hospital stay, and treatment costs.

详细描述

"Huede" AI Aided AKI Prediction Software, Acura AKI, uses machine learning algorithms to predict the risk of AKI within the next 24 hours. It has undergone cross-hospital validation at four medical centers in Taiwan (Taichung Veterans General Hospital, Mackay Memorial Hospital, National Cheng Kung University Hospital, and Kaohsiung Medical University Hospital), successfully obtaining invention patents in Taiwan and the United States, as well as receiving a software medical device license from the Taiwan Food and Drug Administration. Acura AKI is installed on the hospital's servers, where it processes patient physiological data, laboratory parameters, and medication information to infer the risk of AKI occurring within 24 hours. It also provides a ranking of feature importance. By using Acura AKI, physicians can assess the risk of AKI, focusing on high-risk patients to provide care decisions.

This study will be conducted in a prospective randomized clinical trial in adult ICUs, implementing the Acura AKI system for predicting AKI. In the intervention group with Acura AKI system, physicians will be proactively notified via sending alarm message when Acura AKI identifies a high-risk patient population. After receiving alarm message, physicians and pharmacists will provide feedback and recommendations, including blood pressure, fluid management, infusion options, medication adjustment suggestions, and dialysis recommendations. The study aims to determine whether early prediction and intervention using the Acura AKI system can improve the outcomes of critically ill patients with adverse kidney conditions. Additionally, the researchers will collect 20ml of urine from Acura AKI identified patients to test for urinary biomarkers predictive of AKI then verify the performance of Acura AKI with these urinary biomarkers. The study endpoint is to evaluate the cost-effectiveness of using Acura AKI, including the incidence of AKI, dialysis rates, mortality rates, length of hospital stay, and treatment costs.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Participant)

入排标准

年龄范围
20 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Over 20 years old
  • Admitted to adult ICU
  • Hospital stay of more than 30 hours

排除标准

  • Known to have acute kidney injury at enrollment
  • Currently undergoing hemodialysis treatment
  • No available blood or urine test data
  • Pregnant women
  • HIV-positive patients
  • Those who have not provided informed consent form
  • Regarded as unsuitable for inclusion in the trial by the researcher

结局指标

主要结局

Acute kidney injury (AKI) incidence

时间窗: Assessed from time of randomization to time of AKI occurrence (within 7 days post randomization)

Acute kidney injury (AKI) incidence in ICU. AKI is defined by an increase in KDIGO creatinine stage.

次要结局

  • Percentage of recommendations implemented by the primary care team.(24 hours after Randomization)
  • Dialysis rate(Assessed from time of randomization to time of receipt of inpatient dialysis (within 14 days post randomization))
  • Mortality rate(Assessed from time of randomization to date of death from any cause, within 14 days of randomization)
  • Length of hospital stay(Assessed from time of randomization to date of hospital discharge, assessed up to 30 days)
  • Change in treatment costs(Assessed from time of randomization to 60 days post hospital discharge date, accessed up to 90 days)
  • Long term dialysis(From hospital discharge date up to 90 days post discharge date)

研究者

发起方
Huede Healthtech Co., Ltd.
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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