Heart surgery study seeks best way to protect the heart
NCT ID NCT06287372
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study looked at two different methods used to protect the heart during coronary artery bypass surgery. Twenty patients were randomly assigned to receive either Calafiore or modified Del Nido cardioplegic solutions. Researchers measured heart muscle damage markers and amino acid levels during surgery to see which method worked better.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- cardioplegic solutions (Calafiore and modified Del Nido)
- What this could lead to
- If successful, this could help surgeons choose the best method to protect the heart during bypass surgery.
- What could go wrong
- This is a very small, completed study with only 20 patients, so results may not apply to everyone. It looks at lab markers, not long-term patient outcomes.
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
-
20 people
The number who actually took part.
- Started
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Jul 2022
- Finished
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Jul 2023
- 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
Twenty consecutive patients undergoing elective primary coronary artery bypass grafting were enrolled in this study
- 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: * All consecutive patients undergoing elective primary coronary artery bypass grafting were enrolled in this study. Exclusion Criteria: * Patients were excluded from this study if they had suffered from previous myocardial infarction, had reduced ejection fraction or were undergoing combined or repeated surgery.
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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.
Contacts and locations
Locations
-
Damascus University Cardiac Surgery Hospital
Damascus, Syria
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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