Actively Recruiting
Effect of Position and Anesthetic Choice in Intraocular Pressure in Robotic GYN (Gynecologic) Oncology Patients
Led by University of Florida · Updated on 2026-01-16
40
Participants Needed
1
Research Sites
344 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Steep Trendelenburg positioning and insufflation of the abdominal cavity have shown to increase intra ocular pressure. Different anesthetic techniques can alter intra ocular pressure and a small pilot study showed decrease in Intraocular Pressure (IOP) in robotic case in steep Trendelenburg with IV anesthetics (TIVA). We want to quantify the degree of change in Intraocular Pressure (IOP) in female patients undergoing robotic procedures for cancer. We want to detect the difference in increase of pressure with total IV anesthesia versus conventional balanced anesthesia
CONDITIONS
Official Title
Effect of Position and Anesthetic Choice in Intraocular Pressure in Robotic GYN (Gynecologic) Oncology Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female patients 18 years of age or older
- Written informed consent obtained and agreement to follow study procedures
- Planning to receive robotic surgery for gynecological cancer or high suspicion of cancer
- Cleared for surgery by the pre-anesthesia clinic
- All robotic gynecologic cancer patients 18 years and older with any preexisting medical conditions deemed ready for surgery by the pre-anesthesia clinic
You will not qualify if you...
- Known increased intraocular pressure or prior eye surgery within the past month
- Eye conditions preventing intraocular pressure measurement as determined by an ophthalmologist
- Previous treatment for or diagnosis of increased intraocular pressure
- Eye surgery within 30 days prior to consent
- Inability to undergo intraocular pressure measurement as determined by an ophthalmologist
AI-Screening
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Trial Site Locations
Total: 1 location
1
University of Florida
Gainesville, Florida, United States, 32610
Actively Recruiting
Research Team
S
Sonia Mehta, MD
CONTACT
A
Anna Woods
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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