Cheaper brain monitoring method tested in liver transplants
NCT ID NCT07442214
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study compares two non-invasive methods for monitoring brain blood flow during liver transplant surgery: carotid Doppler ultrasound and near-infrared spectroscopy (NIRS). The goal is to see if the simpler, cheaper ultrasound can replace the more expensive NIRS. The study involves 43 adults undergoing elective liver transplantation.
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 simpler, cheaper way to monitor brain blood flow during liver transplant surgery, improving patient safety.
- What could go wrong
- This is a small, early-stage study (43 participants) comparing monitoring 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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43 people
The number who actually took part.
- Started
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Feb 2025
- Expected to finish
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Apr 2026
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
The study population consists of adult patients aged 18-65 years who underwent elective liver transplantation at Inonu University Turgut Ozal Medical Center. All participants had end-stage liver disease and were monitored intraoperatively for cerebral perfusion using carotid Doppler ultrasonography and near-infrared spectroscopy (NIRS). The study was conducted as a single-center, prospective observational study.
- Ages
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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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: * Adult patients aged 18-65 years scheduled for elective liver transplantation * Written informed consent obtained prior to participation Exclusion Criteria: * Fulminant hepatic failure * Hepatic encephalopathy * Hepatorenal or hepatopulmonary syndrome * Pre-existing cerebrovascular disease or carotid stenosis * Severe cardiopulmonary comorbidity * Refusal to participate
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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
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Inonu University Turgut Ozal Medical Center.
Malatya, Battalgazi, 44280, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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