Amino Acids for Cardiac Surgery Associated AKI

{ "Amino Acids for Pediatric Cardiac Surgery AKI", "This study is looking at whether giving amino acids (Trophamine) to children undergoing heart surgery is safe and practical. Some participants will receive a continuous infusion of Trophamine, while others will receive a placebo (lactated ringers solution). The main goal is to see how many participants experience side effects related to the amino acid infusion. This study is for children aged 1 day to 18 years who are having heart surgery and are at high risk for acute kidney injury (AKI). You cannot join if you have certain pre-existing kidney conditions or are already on life support. The study plans to enroll 30 participants, but its current recruitment status is unclear.", "design": "This is an interventional study comparing amino acids to a placebo in about 30 participants. It is not specified if participants or researchers will know which treatment is being given.", "commitments": "Participants will receive a continuous infusion of either amino acids or placebo starting at the time of cardiac surgery and continuing for up to 3 days. Adverse events will be monitored daily during the infusion and for up to 48 hours after it stops (up to 5 days total).", "compensation": "Not stated in the trial record.", "follow_up": "Participants will be monitored for adverse events for up to 5 days after the infusion begins.", }

Study design
Not specified.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Not specified.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07001098

Amino Acids for Cardiac Surgery Associated AKI

Not Yet Recruiting
PHASE2Ages 1–18InterventionalTreatment
Stanford University
~30 participants
Updated 2025-06-03 on ClinicalTrials.gov
What's tested:Amino AcidsPlacebo

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Number of Participants with Amino acids Related Adverse Events
Measured over Baseline, Daily during infusion upto 48 hours after completion of infusion (upto 5 days)
Acute Kidney Injury
1 sites across 1 states
California1
  • Shina Menon, MD · PRINCIPAL_INVESTIGATOR · Stanford University

This trial hasn't published a contact. View it on ClinicalTrials.gov

Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

Undergoing cardiac surgery and expected to be high risk

Exclusion

preoperative extracorporeal organ support
CKD history (GFR\<60ml/min/1.73m2 \[≤1year\] and GFR\<90ml/min/1.73m2 \[\>1 year\])
serum creatinine defined preoperative AKI.
  • Number of Participants with Amino acids Related Adverse EventsBaseline, Daily during infusion upto 48 hours after completion of infusion (upto 5 days)