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Stability Comparison of TIVA and Sevoflurane in Prone Spinal Surgery(TIVA:Total Intravenous Anesthesia)

NCT06558695 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 52

Last updated 2024-08-19

No results posted yet for this study

Summary

Key Points:

1. Objective:

o To compare the effects of Total Intravenous Anesthesia (TIVA) and sevoflurane anesthesia on respiratory mechanics, hemodynamic parameters, and neuromonitoring during prone position spinal surgeries.
2. Methodology:

* A randomized controlled trial involving 52 patients scheduled for lumbar spine surgery, randomly assigned to either TIVA or sevoflurane groups.
* Respiratory and hemodynamic parameters were measured at various time points.
3. Results:

* No significant differences were found between the TIVA and sevoflurane groups in terms of respiratory mechanics or hemodynamic stability.
* Both anesthesia techniques maintained stable intraoperative conditions.
4. Clinical Implications:

* Anesthesiologists can flexibly choose between TIVA and sevoflurane based on patient-specific factors and surgical requirements.
* TIVA may be preferred in surgeries with high neurological risk due to its compatibility with neuromonitoring.
5. Future Research:

* Studies with broader patient populations and long-term outcomes are needed to further refine anesthesia management strategies.
* Research on the environmental impact and cost-effectiveness of anesthesia techniques is also important.

Conditions

  • Spinal Stenosis, Lumbosacral Region

Interventions

DRUG

Sevoflurane

Sevoflurane was managed for maintenance of the general anestesia during spinal surgeries

DRUG

TIVA

TIVA was managed for maintenance of the general anesthesia during spinal surgeries

Sponsors & Collaborators

  • Saglik Bilimleri Universitesi

    lead OTHER

Principal Investigators

  • Yücel Yüce, MD,Assoc Prf · Saglik Bilimleri Universitesi

Study Design

Allocation
RANDOMIZED
Purpose
SCREENING
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-05-01
Primary Completion
2023-06-30
Completion
2024-06-30

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06558695 on ClinicalTrials.gov