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Clinical Trials in Turkey / NCT07642765
Recruiting Observational

EASIX Score and Post-Induction Hypotension in Frail Patients Undergoing Non-Cardiac Surgery

NCT07642765 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-07-01
Last updated
2026-08-04

Condition(s) studied

Hypotension on InductionFrailtyAnesthesia, General

Investigational drug(s) / intervention(s)

EASIX Score Assessment

EASIX Score Assessment: Preoperative Endothelial Activation and Stress Index (EASIX) score calculated from routine laboratory parameters obtained within 24 hours before surgery. Formula: LDH (U/L) × Creatinine (mg/dL) / Platelet count (10⁹/L). No additional blood sampling is performed; only existing routine preoperative laboratory values are used.

Study summary

Post-induction hypotension (PIH) is a common and clinically significant hemodynamic complication following general anesthesia induction. Frail patients are particularly vulnerable due to impaired vascular reactivity and endothelial dysfunction. The Endothelial Activation and Stress Index (EASIX), calculated from routine laboratory parameters (LDH, creatinine, and platelet count), may serve as a preoperative biomarker to identify patients at risk for PIH.

This prospective observational cohort study aims to evaluate the association between preoperative EASIX score and the occurrence of post-induction hypotension in frail patients undergoing elective non-cardiac surgery under general anesthesia. A total of 160 patients with a Clinical Frailty Scale (CFS) score of 4 or above will be enrolled. Mean arterial pressure will be measured every 2 minutes for the first 15 minutes after induction. PIH is defined as MAP below 65 mmHg and/or a decrease of 20% or more from baseline.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age 18 years or older * Scheduled for elective non-cardiac surgery under general anesthesia * Clinical Frailty Scale (CFS) score of 4 or above * Available routine preoperative laboratory values (LDH, creatinine, platelet count) within 24 hours before surgery Exclusion Criteria: * Cardiac surgery * Emergency surgery * Preoperative vasopressor infusion * Severe hematological disease * Missing laboratory data required for EASIX calculation

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Konya City Hospital Konya Turkey (Türkiye) Recruiting

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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 NCT07642765 on ClinicalTrials.gov ↗ ← All trials in Turkey