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

H

Huede Healthtech Co., Ltd.

Status

Enrolling

Conditions

Renal Replacement Therapy
Acute Kidney Injury
Intensive Care

Treatments

Device: Acura AKI

Study type

Interventional

Funder types

Industry

Identifiers

NCT06685367
Huede-113001

Details and patient eligibility

About

"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.

Full description

"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.

Enrollment

3,600 estimated patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

  • 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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

3,600 participants in 2 patient groups

With Acura AKI
Experimental group
Description:
The group with Acura AKI will receive the Acura AKI software, which identifies high-risk AKI patients and sends alert messages to nephrologists and ICU pharmacists. Upon receiving the alert, they will make treatment suggestions.
Treatment:
Device: Acura AKI
Without Acura AKI
No Intervention group
Description:
The group without Acura AKI will be managed based on standard medical procedures.

Trial contacts and locations

1

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Central trial contact

Chun-Te Huang

Data sourced from clinicaltrials.gov

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