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.
Amino Acids for Cardiac Surgery Associated AKI
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Shina Menon, MD · PRINCIPAL_INVESTIGATOR · Stanford University
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- Number of Participants with Amino acids Related Adverse EventsBaseline, Daily during infusion upto 48 hours after completion of infusion (upto 5 days)