Can a simple platelet test predict who bleeds after heart surgery?
NCT ID NCT06961175
First seen Sep 10, 2026 · Last updated Sep 11, 2026 · Updated 1 time
Summary
Researchers are studying whether a preoperative platelet function test can predict heavy bleeding after cardiovascular surgery that uses a heart-lung bypass machine. The study enrolls about 180 adults with normal clotting tests who are not taking antiplatelet drugs and are scheduled for elective bypass surgery. Doctors measure platelet activity with a device called thromboelastography before surgery, then track how much blood collects in chest drains afterward to see if low platelet activity lines up with more bleeding.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If the link holds, doctors could one day use a bedside platelet test before heart surgery to flag patients likely to bleed heavily and plan transfusions or other care in advance.
- What could go wrong
- This is an observational study, so it can show a pattern but cannot prove the test causes better outcomes. Prior studies on this question are small and disagree, and the results may not apply to patients who take antiplatelet 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.
- Participants
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About 180 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2025
- Expected to finish
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Dec 2026
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.
Who is studied
The population undergoing scheduled for cardiovascular surgery at the University Hospital of Salamanca will be taken as the reference population.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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: * Over 18 years of age. * Patients undergoing elective surgery under CPB. * Patients must be duly informed and have signed the informed consent form. * ASA status I-IV. * Sufficient intellectual capacity to understand the procedure. * Normal preoperative coagulation study and platelet count. Exclusion Criteria: * Failure to meet the criteria listed above. * Preoperative administration of antiplatelet agents with an inadequate washout period (5 days for clopidogrel and ticagrelor and 7 days for plasugrel). * Preoperative administration of anticoagulants with an inadequate washout period. * Thrombopenia \<100,000 platelets or anemia \<11 g/dL
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Salamanca University Hospital
RECRUITINGSalamanca, 37007, Spain
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