Ireland
--:--IST
Recruiting Not applicable

Cardiac Index-Guided Intraoperative Hemodynamic Management in Pediatric Moyamoya Surgery

NCT07304947 · tracked via the Priya Life Science South Korea tracker
Phase
Not applicable
Started
2025-12-02
Last updated
2025-12-26

Condition(s) studied

Moyamoya Disease

Investigational drug(s) / intervention(s)

Cardiac Index-Guided Hemodynamic ManagementBlood Pressure-Guided Standard Hemodynamic Management

Cardiac Index-Guided Hemodynamic Management: In the experimental arm, intraoperative hemodynamic management is guided by each patient's baseline cardiac index. Cardiac output is continuously monitored using the LiDCO system after arterial line insertion. Baseline cardiac index is calibrated using transthoracic echocardiography, and intraoperative fluids and vasoactive agents are adjusted to maintain cardiac index within ±20% of baseline. Standard anesthesia monitoring is provided to all patients.

Blood Pressure-Guided Standard Hemodynamic Management: In the control arm, intraoperative hemodynamic management follows conventional blood pressure-guided practice. After arterial line placement, the LiDCO device remains connected but the display is concealed during anesthesia. Fluids and vasoactive medications are adjusted according to standard MAP-based management. Standard anesthesia monitoring is provided to all patients.

Study summary

This prospective randomized controlled trial evaluates whether individualized cardiac index-guided intraoperative hemodynamic management reduces postoperative transient ischemic episodes in pediatric patients undergoing encephaloduroarteriosynangiosis (EDAS) for Moyamoya disease. Patients are randomized 1:1 to goal-directed fluid therapy based on baseline cardiac index versus standard arterial pressure-based management. The primary outcome is the incidence of transient ischemic episodes during hospitalization.

Eligibility

Sex
ALL
Min age
1 Month
Max age
18 Years
Healthy volunteers
No
Inclusion Criteria: * Pediatric patients \<18 years undergoing EDAS for Moyamoya disease under general anesthesia Exclusion Criteria: * ASA physical status 4-5 * Emergency surgery * Known cardiovascular disease * Any condition judged inappropriate by investigators

Primary outcome measure(s)

  • Incidence of transient ischemic episodes during hospitalization — Postoperative hospital stay
    From end of surgery through postoperative hospital discharge, up to 7 days

Trial sites (1)

FacilityCityRegionStatus
Seoul National University Children's Hospital Seoul South Korea Recruiting

Other trials for the same condition

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 NCT07304947 on ClinicalTrials.gov ↗ ← All trials in South Korea