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Recruiting NCT06275308

NCT06275308 Effect of Raised End-Tidal pCo2 on Choroidal Volume

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Clinical Trial Summary
NCT ID NCT06275308
Status Recruiting
Phase
Sponsor University of Pittsburgh
Condition Intraocular Pressure
Study Type INTERVENTIONAL
Enrollment 20 participants
Start Date 2023-02-27
Primary Completion 2026-12-30

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age 8 Years
Study Type INTERVENTIONAL
Interventions
Ventilation manipulation

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 20 participants in total. It began in 2023-02-27 with a primary completion date of 2026-12-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study is to investigate the relationship between arterial carbon dioxide (CO2) concentration and vitreous pressure on the choroidal volume by integrated intraoperative OCT imaging under eye exams under anesthesia.

Eligibility Criteria

Inclusion Criteria: * any child undergoing an eye exam under anesthesia for an ophthalmologic reason. * children between the ages newborn to 8 years of age. Exclusion Criteria: * children who are not having an eye exam under anesthesia. * children with a known medical diagnosis that affect the eye to be studied * \* children over the age of 8 years of age. * \* children with altered cerebral autoregulation, increased intracranial pressure, pulmonary hypertension, or any other condition deemed appropriate by the anesthesiologist. * children in whom a laryngeal mask airway will not be used

Contact & Investigator

Central Contact

Amy Monroe, MPH, MBA

✉ monroeal@upmc.edu

📞 412-623-6382

Principal Investigator

Amy Monroe, MPH, MBA

STUDY DIRECTOR

University of Pittsburgh

Frequently Asked Questions

Who can join the NCT06275308 clinical trial?

This trial is open to participants of all sexes, up to 8 Years, studying Intraocular Pressure. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06275308 currently recruiting?

Yes, NCT06275308 is actively recruiting participants. Contact the research team at monroeal@upmc.edu for enrollment information.

Where is the NCT06275308 trial being conducted?

This trial is being conducted at Pittsburgh, United States.

Who is sponsoring the NCT06275308 clinical trial?

NCT06275308 is sponsored by University of Pittsburgh. The principal investigator is Amy Monroe, MPH, MBA at University of Pittsburgh. The trial plans to enroll 20 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology