Heart surgery fluid trick could cut transfusions and complications
NCT ID NCT07466082
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether using a device called the Pleth Variability Index (PVI) to guide a blood-saving technique (acute normovolemic hemodilution) during heart surgery leads to better fluid balance and fewer complications. Eighty patients undergoing cardiac surgery were enrolled. The goal was to see if PVI guidance reduces the need for blood transfusions and lowers the risk of problems like kidney injury.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- acute normovolemic hemodilution (blood removal and fluid replacement)
- What this could lead to
- If successful, this approach could help heart surgery patients receive fewer blood transfusions and have fewer complications like kidney injury.
- What could go wrong
- This is a small, completed study with 80 participants, so results may not apply to all heart surgery patients. The technique also carries risks of hemodynamic instability if not managed carefully.
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
-
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
-
80 people
The number who actually took part.
- Started
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Nov 2025
- Finished
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Mar 2026
- Lead sponsor
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A government agency
The lead sponsor is a government body.
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 85 years
- Sex
-
Anyone
- Healthy volunteers
-
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: * ASA (American Society of Anesthesiologists) score II-III, * ejection fraction (LVEF) \>45%, * NYHA (New York Heart Association) class I-III, * hematocrit value \>35%, * and patients who have not had a myocardial infarction in the last three months. Exclusion Criteria: * Emergency or redo surgery requirement, * LVEF (left ventricular ejection fraction) \<35%, * severe LMCA (left main coronary artery) stenosis (\>70%), * BMI \<18.5, * severe comorbidity (endocarditis, advanced COPD (chronic obstructive pulmonary disease), CKD (chronic kidney disease), anemia, hypoalbuminemia, peripheral artery disease), * active DAPT /heparin use, * coagulopathy, * uncontrolled systemic diseases, * pregnancy, * malignancy
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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.
Contacts and locations
Locations
-
Bursa City Hospital
Bursa, Nilüfer, 16110, Turkey (Türkiye)
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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