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Clinical Trials in Turkey / NCT07660679
Recruiting Observational

Effect of Preoperative CIMT on Hemodynamics During Liver Transplantation

NCT07660679 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-02-11
Last updated
2026-06-23

Condition(s) studied

Liver TransplantationCarotid Intima-media Thickness

Study summary

Candidates for liver transplantation (CT) carry an increased risk of cardiovascular disease (CVD) due to underlying end-stage liver disease (ESHD) and immunosuppressive drugs used post-transplantation. CVD is a significant cause of long-term mortality after CT \[1\] \[2\]. Carotid Intima-Media Thickness (CIMT), a subclinical marker of atherosclerosis in the preoperative period, is a non-invasive method used to predict future CVD risk \[3\]. High CIMT indicates atherosclerosis and decreased arterial compliance. This can compromise organ perfusion and increase the risk of postoperative complications by increasing intraoperative blood pressure variability (BPV) during anesthesia induction and surgical stress in major surgeries such as CT. Studies investigating whether CIMT is an independent risk factor for perioperative hemodynamic instability in CT patients are limited. The aim of our study is to investigate the effect of CIMT values on intraoperative hemodynamic parameters. Secondary objectives are to determine the association of CIMT with the incidence of hypotension, vasopressor requirement, postoperative acute renal injury (ARI), and major cardiac adverse events (MCAE) after anesthesia induction.

Theoretical Benefit: To make a significant contribution to the literature on the relationship between atherosclerosis and anesthesia management by determining whether CIMT is an independent predictor of perioperative hemodynamic instability in chemotherapy patients.

Practical Benefit: To ensure the inclusion of CIMT measurement in the anesthesia risk assessment of chemotherapy candidates. Identifying patients with high CIMT will guide the implementation of more aggressive and targeted hemodynamic management strategies (e.g., more frequent invasive monitoring, proactive vasopressor use) during anesthesia induction and maintenance.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients aged between 18 and 65 years * Scheduled for elective liver transplantation surgery * Completed preoperative carotid intima-media thickness (CIMT) ultrasonographic measurement * Patients with signed informed consent for data collection Exclusion Criteria: * Patients undergoing emergency liver transplantation * History of previous carotid artery surgery or stenting * Known severe carotid artery stenosis (\>70%) * Severe intraoperative hemodynamic instability prior to induction (e.g., active bleeding or shock) * Incomplete intraoperative advanced hemodynamic monitoring data or vasopressor records

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Dicle University Faculty of Medicine, Department of Anesthesiology and Reanimation Diyarbakır Turkey (Türkiye) Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07660679 on ClinicalTrials.gov ↗ ← All trials in Turkey