Ireland
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Recruiting Observational

Blood Viscosity and Outcomes After Elective Craniotomy

NCT07530393 · tracked via the Priya Life Science South Korea tracker
Phase
Observational
Started
2026-06-23
Last updated
2026-09-14

Condition(s) studied

Postoperative ComplicationsIntracranial Surgery

Investigational drug(s) / intervention(s)

Observational Assessment of Blood Viscosity

Observational Assessment of Blood Viscosity: No intervention is assigned. Intraoperative blood viscosity and clinical variables are measured as part of routine care and analyzed for association with postoperative outcomes.

Study summary

This prospective observational study aims to evaluate the association between intraoperative blood viscosity and postoperative clinical outcomes in adult patients undergoing elective intracranial craniotomy.

Blood viscosity is an important determinant of microcirculatory flow and cerebral perfusion, but its role in perioperative outcomes remains unclear. In this study, intraoperative blood viscosity and related hematologic parameters will be measured, and their relationships with cerebral oxygenation and postoperative complications will be analyzed.

The study will enroll adult patients undergoing elective intracranial surgery at a single tertiary center. The findings of this study may improve understanding of perioperative hemodynamic and hemorheological factors and help identify potential risk markers for adverse postoperative outcomes.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Adults aged 18 to 80 years * Patients scheduled to undergo elective intracranial craniotomy * Patients requiring intraoperative arterial catheterization and routine arterial blood gas analysis * Patients who provide written informed consent Exclusion Criteria: * Emergency surgery * Patients in whom participation or follow-up is considered difficult by the investigator * Patients unable to provide informed consent

Primary outcome measure(s)

  • Number of participants with one or more postoperative composite complications within 30 days after surgery — Up to postoperative day 30
    Composite complication is defined as the occurrence of at least one of the following within 30 days after surgery: postoperative neurologic complications, respiratory complications, cardiovascular complications, acute kidney injury defined as Kidney Disease Improving Global Outcomes stage 1 or higher, infectious complications requiring intravenous antibiotics or a procedure, reoperation or major postoperative intervention, or death.

Trial sites (1)

FacilityCityRegionStatus
Asan Medical Center Seoul Songpa Recruiting
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 NCT07530393 on ClinicalTrials.gov ↗ ← All trials in South Korea