Actively Recruiting
Effect of Combined Intravenous-Inhalational Anesthesia (CIVIA) on Postoperative Recovery Patterns.
Led by Kocaeli City Hospital · Updated on 2025-08-14
210
Participants Needed
1
Research Sites
16 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Effect of Combined Intravenous-Inhalational Anesthesia (CIVIA) on Postoperative Recovery Patterns.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Scheduled for spine surgery
- Expected surgery duration longer than 3 hours
- Use of intraoperative neuromonitoring
- BIS-guided anesthesia administered
- TIVA (with TCI) as the primary anesthetic technique
- Age >18 years
You will not qualify if you...
- Emergency surgeries
- Patients receiving sole inhaled anesthesia (no TIVA)
- Perioperative dural injury
- Intraoperative severe hypotension requiring inotropic support
- Hypothermia (based on temperature measured before recovery)
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Kocaeli City Hospital
Kocaeli, Izmıt, Turkey (Türkiye), Yozgat
Actively Recruiting
Research Team
A
Ahmet YUKSEK, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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