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Active, Not Recruiting

NCT Number: NCT07442214

View of Cerebral Perfusion in Liver Transplantation

Investigator's aim in this study is to compare the more accessible and low-cost Carotid Doppler USG measurements, which are relatively more difficult to access, costly, and have technical disadvantages, and to demonstrate their superiority over each other in the evaluation of cerebral perfusion in liver transplantation surgeries, without any invasive intervention to the patient.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Inonu University Turgut Ozal Medical Center.

Malatya, Battalgazi, 44280, Turkey (Türkiye)

About this study

Liver transplant surgeries cause intraoperative problems that are difficult to manage from hemodynamic, respiratory, neurological, hematological, and metabolic perspectives due to the nature of liver failure, which affects many organs and systems. Particularly during the anhepatic period, when the healthy graft is integrated into the recipient's vascular system, clamping of the inferior vena cava, one of the two main veins of the hepatic veins, is often required for its connection. This means that a sudden interruption occurs in the blood volume returning to the heart from the lower part of the body, which constitutes half of the total cardiac output.

Cerebral perfusion is also affected during the anhepatic period, and previous studies have observed impaired cerebral perfusion using cerebral oximetry. However, not every clinic has a cerebral oximetry device, and there are factors that limit its use. Some of these factors include high cost, hyperbilirubinemia, variables that disrupt regional blood flow, diabetes, hypertension, and low hemoglobin.

Ultrasound devices are more commonly available in large clinical centers that perform liver transplant surgeries, even for other purposes. It is possible to evaluate the blood flow to the brain using carotid Doppler ultrasonography. The aim of this study is to measure patients' carotid peak systolic and end-diastolic flow and carotid peak systolic flow variability using carotid Doppler ultrasonography and to compare these measurements with cerebral oximetry measurements.

Translated with DeepL.com (free version)

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Carotid Doppler Ultrasonography and Near-Infrared Spectroscopy (NIRS)

Device

Non-invasive intraoperative monitoring of cerebral perfusion using NIRS and carotid Doppler.

Primary outcomes

  1. PSv

    Time frame: During surgery: T0: Preanhepatic phase T1: Anhepatic phase T2: Neohepatic phase

    peak systolic velocity (PS) cm/sec)

  2. rSO₂

    Time frame: During surgery: T0: Preanhepatic phase T1: Anhepatic phase T2: Neohepatic phase

    regional cerebral oxygen saturation (%)

Secondary outcomes

  1. PPV

    Time frame: During surgery: T0: Preanhepatic phase T1: Anhepatic phase T2: Neohepatic phase

    pulse pressure variation (%)

  2. CI

    Time frame: During surgery: T0: Preanhepatic phase T1: Anhepatic phase T2: Neohepatic phase

    cardiac index (L/min/m2)

Sponsors and collaborators

Lead sponsor

Inonu University

Other

Registry information

Official study title

Comparison of Carotid Doppler Ultrasonography With Cerebral Oximetry in Assessing Cerebral Perfusion in Liver Transplantation Surgery

Acronym: NIRS/Doppler

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Mar 2, 2026
Registry last updated
Mar 2, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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