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RECRUITING
NCT05988658

Combining Biomarkers and Electronic Risk Scores to Predict AKI in Hospitalized Patients

Sponsor: University of Chicago

View on ClinicalTrials.gov

Summary

The study's objective is to evaluate the additive value of renal biomarkers (from blood and urine) for identifying individuals at high risk for severe acute kidney injury (AKI) above that of a novel natural language processing (NLP)-based AKI risk algorithm. The risk algorithm is based on electronic health records (EHR) data (labs, vitals, clinical notes, and test reports). Patients will enroll at the University of Chicago Medical Center and the University of Wisconsin Hospital, where the risk score will run in real time. The risk score will identify those patients with the highest risk for the future development of Stage 2 AKI and collect blood and urine for biomarker measurement over the subsequent 3 days.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

800

Start Date

2024-01-05

Completion Date

2028-03-01

Last Updated

2025-09-12

Healthy Volunteers

No

Interventions

DEVICE

ESTOP - AKI 2.0

Medical software as a Noninvasive medical device, which at the time of the project will not implement directly into subject/clinical care.

Locations (2)

University of Chicago Medical Center

Chicago, Illinois, United States

University of Wisconsin Hospital

Madison, Wisconsin, United States