Actively Recruiting

Phase 4
Age: 18Years +
All Genders
Healthy Volunteers
NCT07123870

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

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Kocaeli City Hospital

Kocaeli, Izmıt, Turkey (Türkiye), Yozgat

Actively Recruiting

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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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