Heart surgery anesthesia showdown: can ketamine shield kidneys better than propofol?
NCT ID NCT05268562
First seen Jun 26, 2026 · Last updated Jul 14, 2026 · Updated 3 times
Summary
This study tests whether using ketamine or propofol for anesthesia at the start of heart surgery affects the risk of acute kidney injury. Researchers will enroll 200 adults undergoing complex heart surgery with a heart-lung machine. The goal is to see which drug leads to fewer kidney problems and better stability during surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ketamine and propofol
- What this could lead to
- If ketamine proves better, it could become the preferred anesthetic for heart surgery to reduce kidney damage.
- What could go wrong
- This is a single-center Phase 4 trial with 200 participants, so results may not apply broadly. The study is active but not recruiting, and findings may show no difference between the drugs.
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.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
About 200 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Mar 2022
- Expected to finish
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Jun 2027
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.
- Ages
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70 years and older
- Sex
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Anyone
- Healthy volunteers
-
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: * Presenting for cardiac surgery at the Mayo Clinic in Rochester, Minnesota. * Scheduled to undergo complex cardiac surgery with the use of cardiopulmonary bypass. Complex cardiac surgery will be defined as surgery involving more than one heart valve, redo-sternotomy procedures, or combined valvular and coronary artery bypass graft procedures (aortic repair not excluded if meets other criteria). Exclusion Criteria: * Left or right ventricular assist device implantation or explantation. * Procedures not requiring cardiopulmonary bypass. * Active infection or sepsis requiring antimicrobial therapy and/or vasopressor therapy (treated endocarditis is not excluded). * Severe hepatic disease resulting in ascites. * Pre-operative significant renal dysfunction including a baseline creatinine equal to or greater than 2 mg/dL or requiring dialysis. * Immunosuppressive medication use (including current IV or oral steroids use, use of anti-rejection medications for transplant within 1 month, or chemotherapy within 6 months). * Immunodeficiency syndrome including HIV/AIDS, leukemia, and multiple myeloma
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Mayo Clinic in Rochester
Rochester, Minnesota, 55905, United States
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