A common amino acid may shield kidneys after heart surgery — a massive analysis puts it to the test
NCT ID NCT07718373
First seen Jul 22, 2026 · Last updated Aug 11, 2026 · Updated 3 times
Summary
Acute kidney injury is a frequent and serious complication after cardiac surgery, and effective prevention remains elusive. This study analyzes data from 5,000 adults who had heart surgery with a heart-lung machine to see whether giving the amino acid L-arginine within the first three days after surgery lowers their risk of kidney damage. L-arginine is a building block for nitric oxide, a molecule that helps blood vessels relax and may improve kidney blood flow.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- the amino acid L-arginine given intravenously within the first three days after heart surgery
- What this could lead to
- If L-arginine proves protective, it could offer a simple, low-cost way to reduce kidney damage after cardiac surgery.
- What could go wrong
- This is an observational analysis, not a randomized trial, so results may be influenced by other factors. L-arginine can also cause side effects like low blood pressure or electrolyte imbalances.
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 5,000 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Aug 2026
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
adults admitted to the ICU after CPB-assisted cardiac surgery
- Ages
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18 years and older
- 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: ·adults admitted to the ICU after CPB-assisted cardiac surgery Exclusion Criteria: * congenital heart disease, * surgery requiring deep hypothermic circulatory arrest, * a preoperative baseline estimated glomerular filtration rate (eGFR) below 30 mL/min/1.73 m², * AKI already present prior to ICU 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 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.
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Other studies related to the condition(s) this trial covers.
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