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Search / Trial NCT03644641

The Influence of Prone Position for Spinal Surgery on Visual Acuity

Launched by UNIVERSITY HOSPITAL HRADEC KRALOVE · Aug 22, 2018

Trial Information

Current as of August 21, 2025

Not yet recruiting

Keywords

Desflurane Near Infrared Spectroscopy Propofol Spinal Surgery Prone Position Visual Acuity Visual Loss

ClinConnect Summary

This clinical trial is looking at how two types of anesthesia, desflurane and propofol, affect vision in patients who are lying on their stomachs during spinal surgery. The researchers want to understand if one of these anesthetics might be better at keeping eye pressure lower, which could help preserve vision quality after surgery.

To participate in this study, you would need to be between the ages of 18 and 75 and have a good level of alertness, as indicated by a score of 15 on the Glasgow Coma Scale. You should also be in good overall health, as defined by a classification system used by anesthesiologists. Participants should be undergoing spinal surgery that lasts less than three hours and should have a normal heart rhythm. However, if you have a serious neurological condition, lung disease, or a known allergy to propofol, you would not be eligible for this trial. The study is not yet recruiting participants, but it's designed to help improve our understanding of how anesthesia can affect vision during surgery.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Glasgow Coma scale 15
  • American Society of Anesthesiologists (ASA) Physical Status Classification System I-III
  • spinal surgery in duration less than 3 hours
  • sinus rhythm
  • Exclusion Criteria:
  • postoperative artificial ventilation
  • serious neurological disease
  • lung disease with hypercapnia
  • propofol allergy

About University Hospital Hradec Kralove

University Hospital Hradec Králové is a leading academic medical center in the Czech Republic, renowned for its commitment to advancing healthcare through innovative research and clinical trials. As a prominent sponsor of clinical studies, the hospital integrates cutting-edge medical practices with rigorous scientific inquiry, fostering collaborations that enhance patient care and treatment outcomes. With a multidisciplinary team of experts, state-of-the-art facilities, and a strong emphasis on ethical standards and patient safety, University Hospital Hradec Králové plays a pivotal role in translating research findings into practical applications that benefit the broader medical community.

Locations

Hradec Kralove, , Czechia

Patients applied

0 patients applied

Trial Officials

Pavel Dostal, MD, Ph.D.

Study Director

Hradec Kralove, Czechia 50005

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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