Actively Recruiting
Effect of Raised End-Tidal pCO2 on Choroidal Volume in Children Undergoing Eye Exams Under Anesthesia
Led by University of Pittsburgh · Updated on 2026-01-09
20
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to understand how changes in the amount of carbon dioxide in the blood affect the pressure inside the eye and the thickness of the choroid, the layer of blood vessels between the retina and sclera. The study focuses on children up to 8 years old undergoing eye exams or non-intraocular eye procedures while under anesthesia. It explores whether increased vitreous pressure during surgery is related to changes in choroidal volume, which may cause complications. During the study, children's end tidal carbon dioxide levels will be adjusted to specific targets (30, 40, and 50 mmHg) during anesthesia. After holding each level for five minutes, the pressure inside the eye will be measured with a pneumatonometer, and three scans of the choroid will be taken using an integrated optical coherence tomography (OCT) device built into the operating microscope. Measurements of the eye's axial length and positioning checks ensure accurate and consistent imaging. Participants will have their eye examined once consent is given while under anesthesia. The study involves multiple evaluations of intraocular pressure and choroidal thickness at each carbon dioxide level. Researchers will monitor these measurements to understand their relationship. The total participation duration aligns with the timing of the exam and the ventilation changes, with careful monitoring throughout. The study is sponsored by the University of Pittsburgh and will continue until December 2026.
CONDITIONS
Brief Title
Effect of Raised End-Tidal pCo2 on Choroidal Volume
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Children undergoing an eye exam under anesthesia for an ophthalmologic reason
- Children between newborn and 8 years of age
You will not qualify if you...
- Children not having an eye exam under anesthesia
- Children with a known medical diagnosis affecting the eye to be studied
- Children over 8 years of age
- Children with altered cerebral autoregulation, increased intracranial pressure, pulmonary hypertension, or other conditions as deemed by the anesthesiologist
- Children in whom a laryngeal mask airway will not be used
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Single procedure visit
Participants undergo anesthesia for an eye exam or a non-intraocular eye procedure during which end tidal carbon dioxide levels are manipulated to 40mmHg, 30mmHg, and 50mmHg. At each level, after at least 5 minutes, intraocular pressure is measured and choroidal images are taken using Optical Coherence Tomography (OCT). Additional measurements include axial length of the eye using ultrasound and positioning verification with a spirit level.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
University of Pittsburgh Medical Center
Pittsburgh, Pennsylvania, United States, 15224
Actively Recruiting
Research Team
A
Amy Monroe, MPH, MBA
A
Alisha Maslanka, BS, CCRC
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
BASIC_SCIENCE
Number of Arms
1
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