Can a computer measure heart strain as well as a doctor during surgery?
NCT ID NCT07496424
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looks at whether new, fully automated software can measure heart muscle strain as accurately as the current manual method during heart surgery. The manual method takes about 5 minutes, which is often too slow in the operating room. The automated method takes just seconds. Researchers will enroll 70 adult heart surgery patients and compare the two measurement techniques.
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 automated strain analysis proves reliable, it could speed up heart function assessment during surgery, helping doctors make faster decisions.
- What could go wrong
- This is a small, early-stage observational study (70 participants) comparing measurement methods, not testing a treatment. Results may not apply to all patients or settings.
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 70 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Mar 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 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 undergoing cardiac surgery who are monitored with a transesophageal echocardiography probe
- Ages
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18 to 99 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: * Adult (≥18 years) cardiac surgery patients * Sinus rhythm * No severe valvular regurgitation * Use of General Electric (GE) echocardiography systems (Vivid S60, S70, E95) and corresponding EchoPAC software as well as TOMTEC software. Exclusion Criteria: * Inadequate image quality * Any severe heart valve regurgitation * Mechanical circulatory support systems (e.g., LVAD, Impella, ECMO)
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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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General Hospital of Vienna - Medical University of Vienna
RECRUITINGVienna, 1090, Austria
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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