Can a squirt of heart medicine boost bypass success?
NCT ID NCT06301880
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether applying the drugs milrinone or nitroglycerin directly onto a blood vessel used in heart bypass surgery could improve blood flow. Forty-six patients having elective bypass surgery were randomly assigned to receive one of the two drugs or a saltwater solution. The goal was to see if either drug increased blood flow from the internal mammary artery during the operation.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- milrinone or nitroglycerin
- What this could lead to
- If it works, this could point toward a simple way to improve blood flow during heart bypass surgery, potentially leading to better surgical outcomes.
- What could go wrong
- This is a small, completed trial with only 46 participants, so results may not apply to all patients. The intervention is applied during surgery and only affects blood flow at that moment, not long-term health.
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 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
-
46 people
The number who actually took part.
- Started
-
Jan 2022
- Finished
-
Jan 2023
- Lead sponsor
-
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
-
Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
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: * patients undergoing elective primary coronary artery bypass grafting Exclusion Criteria: * patients who developed ischemic events during 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
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