A quick clotting test could make transfusions safer for children in surgery
NCT ID NCT05379530
First seen Aug 14, 2026 · Last updated Aug 14, 2026
Summary
This study looks at whether a rapid blood test called thromboelastography (TEG) can help doctors manage bleeding during high-risk surgeries in children. TEG measures how well blood clots in real time, which might guide decisions about which blood products to give. The study will observe children undergoing surgeries with a high chance of needing a transfusion, such as spinal or major abdominal surgery, and compare transfusion practices to historical data. The goal is to see if TEG helps doctors use the right type and amount of blood products, potentially improving safety.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Thromboelastography (TEG), a point-of-care blood test that assesses clotting function during surgery
- What this could lead to
- If TEG proves useful, it could help doctors give the right blood products to children during major surgery, reducing complications from too few or too many transfusions.
- What could go wrong
- This is a small, single-center observational study, so results may not apply broadly. TEG is not yet standard for pediatric non-cardiac surgery, and its impact on outcomes remains uncertain.
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
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2027
An estimate. Start dates often move.
- Expected to finish
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Dec 2028
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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Up to 20 years
- 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: * Pediatric patients undergoing non-cardiac surgery at BCH with a high likelihood of blood transfusion. Specifically these are defined as a surgery with greater than 25% likelihood of transfusion of any non-albumin blood product. * Eligible surgeries include: * spinal surgery * laparotomy * liver transplant * craniofacial surgery * esophageal atresia * craniotomy/hemispherectomy * major abdominal surgery * major hip surgery * major plastic surgery Exclusion Criteria: * Patients undergoing cardiac surgery or ECMO cannulation, as these surgeries are generally considered outside the scope of general pediatric surgery. * Patients presenting for emergent surgery * Patients undergoing surgeries off hours (between 8pm and 8 am), when TEG analysis is unobtainable
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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 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.
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Other studies related to the condition(s) this trial covers.
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