AI aims to cut blood waste in surgery prep
NCT ID NCT07223853
First seen Jun 27, 2026 · Last updated Aug 28, 2026 · Updated 2 times
Summary
This study tests a computer system that helps doctors decide which patients need blood prepared before surgery. About 1 million patients in the US need blood transfusions during surgery each year, but often too much blood is prepared, leading to waste. The system uses patient data to predict who really needs blood. The trial involves 50 patients and compares the smart system to usual care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- S-PATH clinical decision support system
- What this could lead to
- If successful, this system could help hospitals better match blood preparation to patient needs, reducing waste and costs while maintaining safety.
- What could go wrong
- This is a small, early-stage trial with only 50 participants, so results may not apply broadly. The system may not improve outcomes or could be difficult to implement in other hospitals.
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 50 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2025
- Expected to finish
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Jan 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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18 years and older
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Clinician Level Exclusion Criteria: * Clinician (resident physician or advanced practice provider) who works at a preoperative assessment clinic Clinician Level Exclusion Criteria: * None Patient Inclusion Criteria: * Scheduled for surgery in one of the main operating room areas (non-remote) at Barnes Jewish Hospital * Evaluated in-person at one of the preoperative assessment clinics affiliated with BJC Healthcare * Have a valid S-PATH model prediction prior to their preoperative assessment clinic visit Patient Exclusion Criteria: * Pregnant * Presence or history of red cell alloantibodies
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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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Washington University / Barnes Jewish Hospital
RECRUITINGSt Louis, Missouri, 63110, United States
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