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Not Yet RecruitingNCT03644641

The Influence of Prone Position for Spinal Surgery on Visual Acuity

The Influence of Prone Position for Spinal Surgery on Visual Acuity, a Comparison of Volatile Anesthesia With Desflurane to Total Intravenous Anesthesia With Propofol

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
University Hospital Hradec Kralove · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This study investigated the effect of desflurane and propofol anesthesia on visual acuity in patients in prone position for spinal surgery. Many trials have investigated the effects of different anesthetic agents on intraocular pressure, propofol may reduce intraocular pressure more than other intravenous anesthetics.

Detailed description

Perioperative increase in intraocular pressure can be caused by prone positioning. In addition to surgical factors, patients with glaucoma, uncontrolled hypertension, arthrosclerosis, and morbid obesity are at risk for potentially damaging optic nerve and loss of optic nerve function. Some studies found that intraocular pressure values were significantly lower in patients undergoing propofol total intravenous anesthesia than in patients undergoing desflurane anesthesia during intraoperative positional changes. Pronounced vasodilatation caused by desflurane might produced hyperaemia with higher intraocular pressure. Hemodynamic response to prone position measured by near-infrared spectroscopy (NIRS) on the prefrontal cortex could determine changes caused by prone position.

Conditions

Interventions

TypeNameDescription
PROCEDUREDesflurane GroupGeneral anesthesia will be held using desflurane in end- tidal concentration according to target value of entropy levels (between 40 and 60).
PROCEDUREPropofol GroupGeneral anesthesia will be held using Schnider effect model for propofol (target control anesthesia). Titration will be done according to target value of entropy levels (between 40 and 60).

Timeline

Start date
2025-11-28
Primary completion
2028-11-30
Completion
2029-12-30
First posted
2018-08-23
Last updated
2024-05-10

Locations

1 site across 1 country: Czechia

Source: ClinicalTrials.gov record NCT03644641. Inclusion in this directory is not an endorsement.