Trials / Not Yet Recruiting
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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Desflurane Group | General anesthesia will be held using desflurane in end- tidal concentration according to target value of entropy levels (between 40 and 60). |
| PROCEDURE | Propofol Group | General 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.