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Search / Trial NCT07067008

Measurement of Intraocular Pressure in Patients Undergoing Laminectomy in the Prone Position

Launched by ELAZIG FETHI SEKIN SEHIR HASTANESI · Jul 4, 2025

Trial Information

Current as of July 22, 2025

Not yet recruiting

Keywords

Prone Position Intraocular Pressure Laminectomy

ClinConnect Summary

This clinical trial is studying how eye pressure changes in patients having a type of back surgery called laminectomy, where the patient lies face down (prone position) during the procedure. Sometimes, being in this position can increase pressure inside the eye, which is rare but could potentially cause serious problems like vision loss after surgery. The study will use a special, gentle device that measures eye pressure without touching the eye, to see how the pressure changes during surgery and to understand what factors, like anesthesia or patient characteristics, might affect these changes.

People who might be eligible to join are adults scheduled for laminectomy surgery under general anesthesia, who are generally healthy enough for surgery (rated ASA I to III), do not have eye diseases like glaucoma, and can cooperate after the surgery. Participants will have their eye pressure measured several times during the surgery using the non-contact device. This information will help doctors find better ways to manage anesthesia and positioning during surgery to keep patients’ eyes safe. If you fit these criteria and agree to take part, the study team will closely monitor your eye health as part of your care.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Patients scheduled for laminectomy surgery under general anesthesia
  • Patients with ASA physical status I-II-III
  • Patients who can cooperate postoperatively
  • Patients without eye diseases or conditions affecting eye physiology (such as glaucoma)
  • Patients who have not undergone eye surgery
  • Patients who consent to participate in the study
  • Exclusion Criteria:
  • Patients scheduled for laminectomy surgery but not receiving general anesthesia
  • Patients with ASA physical status IV-V
  • Patients who do not consent to participate in the study
  • Patients who cannot cooperate postoperatively
  • Patients with eye diseases or conditions affecting eye physiology (such as glaucoma)
  • Patients who have undergone eye surgery
  • Patients from whom consent cannot be obtained

About Elazıg Fethi Sekin Sehir Hastanesi

Elazığ Fethi Sekin City Hospital is a prominent healthcare institution dedicated to advancing medical research and improving patient outcomes through innovative clinical trials. Located in Elazığ, Turkey, the hospital is equipped with state-of-the-art facilities and a multidisciplinary team of healthcare professionals committed to conducting high-quality research in various therapeutic areas. By fostering collaboration between researchers, healthcare providers, and patients, Elazığ Fethi Sekin City Hospital aims to contribute significantly to the development of new treatments and enhance the understanding of various medical conditions within the community and beyond.

Locations

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported