New monitoring method may help doctors manage blood pressure during heart surgery
NCT ID NCT02652858
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study measured how fast pulse waves travel from the heart to different arteries in 40 patients undergoing heart surgery with a heart-lung machine. The goal was to see if this speed can detect when blood pressure in central arteries differs from that in arm or leg arteries. Researchers used non-invasive arm and leg cuffs plus a standard wrist catheter to track these changes.
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 improve how doctors monitor blood pressure during heart surgery, potentially leading to better decisions about medication.
- What could go wrong
- This is a small, observational study with only 40 participants, so results may not apply to all patients. It does not test a treatment, so direct patient benefit is not expected.
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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40 people
The number who actually took part.
- Start date
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Jan 2016
- Finished
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Sep 2016
- 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 to 80 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.
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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.
Inclusion Criteria: * Scheduled patient for coronary or valvular surgery with cardiopulmonary bypass * Cardiopulmonary bypass is at least 90 minutes * Written consent is needed Exclusion Criteria: * Patient with heart rate disorder * Patient with aortic dissection * Dobutamine/milrinone/levosimendan treatment before surgery * Patient with heart rate due to a pacemaker
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Hospices Civils de Lyon
Bron, 69500, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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