Clinical Trial

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

Completed Phase 4
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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.
Protocol Amendment History 1 change
critical Trial completed 2026-08-06
Trial Details
NCT Number NCT07123870
Lead Sponsor Kocaeli City Hospital
Conditions Postoperative Recovery, Inhalation Anesthesia, Total Intravenous Anesthesia
Enrollment 210 participants
Start Date 2025-07-23
Primary Completion 2025-11-12 (estimated)
Study Completion 2025-11-15 (estimated)
Updated on ClinicalTrials.gov 2026-08-05