A simple urine test and a smart alert may help predict kidney failure in sick kids
NCT ID NCT07718464
First seen Jul 22, 2026 · Last updated Jul 23, 2026 · Updated 1 time
Summary
This study tests whether adding a clinical decision support tool to the electronic medical record helps doctors use the furosemide stress test in critically ill children at high risk for acute kidney injury. The furosemide stress test measures how the kidneys respond to a diuretic, which may predict whether a child will need dialysis. Researchers will compare outcomes in the two years after the tool is introduced with the two years before, focusing on fluid buildup and the need for kidney replacement therapy.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a clinical decision support tool for the furosemide stress test
- What this could lead to
- If successful, this tool could help doctors identify children at risk for severe kidney injury earlier and reduce dangerous fluid buildup, potentially avoiding the need for dialysis.
- What could go wrong
- This is a single-center study comparing outcomes before and after the tool is introduced, not a randomized trial, so other factors could influence results. The tool itself does not treat kidney injury—it only guides testing.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 120 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2026
- Expected to finish
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Jun 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Critically ill patients admitted to the PICU at Cincinnati Children's Hospital Medical Center identified as being high risk for developing AKI (RAI+/NGAL+)
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Admitted to the pediatric intensive care unit (PICU) * Renal Angina Index (RAI) greater than or equal to 8 (RAI+) * Urine NGAL greater than or equal to 150 ng/mL (NGAL+) Exclusion Criteria: * Receipt of renal replacement therapy prior to PICU admission
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Cincinnati Children's Hospital Medical Center
RECRUITINGCincinnati, Ohio, 45229, United States
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Other studies related to the condition(s) this trial covers.
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- Can better nurse training reduce ICU complications?
- Ultrasound could guide safer fluid dosing after heart surgery
- Can a heart drug rescue failing kidneys in the ICU?