drugset / Trial / NCT07123870

Effect of Combined Intravenous-Inhalational Anesthesia (CIVIA) on Postoperative Recovery Patterns.

NCT07123870

Phase 4 Recruiting 210 enrolled Kocaeli City Hospital
RandomizedParallel-groupDouble-blindTreatment

Summary

This study was planned as a single-center, prospective, randomized trial. Adult patients undergoing elective spinal surgery lasting longer than three hours, performed in a neurosurgery operating room, will be evaluated. Patients managed with three different anesthesia methods currently used will be examined for recovery patterns: 1. Total intravenous anesthesia (TIVA), 2. TIVA Combined anesthesia with sevoflurane and intravenous agents (sevoflurane-CIVIA), 3. TIVA Combined anesthesia with desflurane and intravenous agents (desflurane-CIVIA). Recovery patterns include; extubation time, eye opening time, emergence agitation, postoperative nausia and vomiting and postoperative recovery unit discharge time.

Timeline

Start
2025-07-23
Primary completion
2025-10-29
Completion
2025-11-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Desflurane Other / unclassified 0.5 unknown Inhaled
Subject Sevoflurane Other / unclassified 0.5 unknown Inhaled
Background Propofol Small molecule 2 ug/ml Intravenous
Background Propofol Small molecule 4 ug/ml Intravenous
Background Remifentanil Small molecule 1 ng/ml Intravenous
Background Remifentanil Small molecule 4 ng/ml Intravenous

Indications

No indication recorded.