Actively Recruiting

Age: 18Years +
All Genders
NCT06496555

Evaluation of U-AKIpredTM for Predicting AKI in Critically Ill Patients Within 12 Hours: a Multicenter Prospective Cohort Study

Led by Second Affiliated Hospital, School of Medicine, Zhejiang University · Updated on 2024-07-11

2100

Participants Needed

1

Research Sites

82 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of our study is to evaluate U-AKIpredTM for predicting AKI in critically ill patients within 12 h by the multicenter prospective cohorts. AKI was diagnosed by Kidney Disease Improving Global Outcomes (KDIGO) criteria. We designed five aspects including the overall fitting effecience evaluation, calibration curve, quantifying calibration performance, quantifying discrimination performance, quantifying clinical utility to evaluate the external validation model.

CONDITIONS

Official Title

Evaluation of U-AKIpredTM for Predicting AKI in Critically Ill Patients Within 12 Hours: a Multicenter Prospective Cohort Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Critically ill patients who have stayed in the intensive care unit (ICU) for over 24 hours
  • Patients aged 18 years or older
Not Eligible

You will not qualify if you...

  • Patients diagnosed with acute kidney injury before or upon ICU admission
  • Patients diagnosed with acute kidney disease before or upon ICU admission
  • Patients diagnosed with chronic kidney disease before or upon ICU admission
  • Patients who have undergone kidney dialysis before or upon ICU admission
  • Patients who have undergone kidney transplantation before or upon ICU admission
  • Pregnant women

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

2nd Affiliated Hospital, School of Medicine, Zhejiang University

Hangzhou, Zhejiang, China

Actively Recruiting

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Research Team

T

Tao Sun, Doctor

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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