AI reads ultrasound videos to predict blood volume
NCT ID NCT06957587
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study aims to develop an AI model that estimates a patient's blood volume from ultrasound videos of major blood vessels. Researchers will record ultrasound clips from 800 adults scheduled for surgery and compare them to a reliable blood volume measurement. The goal is to create a non-invasive tool that could improve fluid management during surgery.
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 successful, this could lead to a quick, non-invasive way to measure blood volume before surgery, helping doctors manage fluids more precisely.
- What could go wrong
- This is an early observational study, not a treatment trial. The AI model may not work accurately in all patients, and results need validation before clinical use.
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 800 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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Aug 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.
Who is studied
Patients prepare to receive surgery.
- Ages
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18 to 75 years
- 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: * Agree to join this study and sign the informed consent form; * Age between 18 and 75 years old (inclusive); * BMI (body mass index) is between 18 and 30 kg/m2; * American Society of Anesthesiologists (ASA) grades I-II Exclusion Criteria: * Preoperative hemoglobin (Hb) \<10g/dl * Cardiac dysfunction (NYHA class III-IV), respiratory dysfunction (ATS class 2-4), history of liver and kidney dysfunction (such as transaminase / albumin / bilirubin abnormalities, hepatitis history, serum creatinine / urea nitrogen rise, etc.), nervous system abnormalities (those who cannot cooperate due to stroke or its sequelae, Alzheimer, etc.); * The ultrasonic display of inferior vena cava, internal jugular vein, subclavian vein or common carotid artery is extremely poor, venous thrombosis or anatomical abnormalities; * Multiple injury with chest, abdomen or brain; * Pregnant woman
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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
2 sites. 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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Shanghai Jiao Tong University Affiliated Sixth People's Hospital
NOT_YET_RECRUITINGShanghai, Shanghai Municipality, 200235, China
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Shanghai Jiao Tong University Affiliated Sixth People's Hospital
RECRUITINGShanghai, Shanghai Municipality, 200235, China
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