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Peripheral Choroidal Layer Response

Peripheral Choroidal Response to Pure Defocus and Oriented Blur Conditions

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05132140
Enrollment
40
Registered
2021-11-24
Start date
2021-11-30
Completion date
2023-05-31
Last updated
2021-11-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myopia

Brief summary

The study aims to examine how the vascular layer of the eyeball (choroidal layer) responds when part of the visual field is exposed to specially generated visual stimulus. The study goal will be accomplished by producing specific blur visual stimulus at a particular visual field position and measure any consistent thickness change pattern in the choroidal layer. We propose to test the hypothesis that regional changes in the choroidal thickness may be induced differently after short-term exposure to specific visual stimuli.

Interventions

DEVICEadaptive optics system

the system consists of a wavefront sensor and a deformable mirror that measure and correct (or modify) the eye's optical imperfections (aberrations).

Sponsors

University of Houston
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

A person is eligible for inclusion in the study if he/she: * Is between the ages of 18 and 40 yrs old * Has normal best corrected visual acuity being 20/20 or better * Has spherical refractive error between +1.00D and -6.00D. * Is capable of fixating on the target. * Has no prior ocular surgery. * Has no ocular pathology except keratoconus. * Can tolerate dilating eye drops

Exclusion criteria

A person will be excluded from the study if he/she: * Does not fall within above mentioned age group. * Has chronic or systemic eye disease that would interfere with pupil dilation via eye drops. * Underwent ocular surgeries or history of ocular trauma * Has shallow anterior chamber angle and/or glaucoma. * Has clinically significant dry eye. * Has signs of any choroidal or retinal pathology, and abnormalities in the visual pathway * Has spherical refractive error that exceeds the limits outlined above. * Has binocular anomalies (e.g. convergence insufficiency, strabismus, pseudo-myopia, amblyopia). * Is an adult unable to consent * Is an individual who is not yet adult (infants, children, teenagers) * Is a pregnant woman * Is a prisoner * Is a student for whom you have direct access to/influence on grades * Is an economically and/or educationally disadvantaged person

Design outcomes

Primary

MeasureTime frameDescription
choroidal thicknessup to 60 minsA commercially available optical coherence tomography system will be used to measure changes in choroidal layer thickness before and after manipulating the peripheral optics.

Contacts

Primary ContactGeunyoung Yoon, PhD
gyoon2@central.uh.edu7137437860
Backup ContactDibyendu Pusti, PhD
dpusti@central.uh.edu5854069837

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026