Actively Recruiting

Phase Not Applicable
Age: 0 - 8Years
All Genders
Healthy Volunteers
ID06275308

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

Age: 0 - 8Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Children undergoing an eye exam under anesthesia for an ophthalmologic reason
  • Children between newborn and 8 years of age
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

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

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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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