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To Study the Effects of Refractive Surgery on OCT Measurements in the Eye

To Study the Effects of Refractive Surgery on Optical Coherence Tomography (OCT) Measurements in the Eye: A Pilot Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05856786
Enrollment
33
Registered
2023-05-12
Start date
2024-06-01
Completion date
2027-12-01
Last updated
2026-08-26

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

Conditions

Myopia, Optical Coherence Tomography, Refractive Errors

Brief summary

Corrective eye surgeries, such as Lasik, are widely used to correct focusing problems such as myopia, or nearsightedness. Often these patients develop other conditions like myopic maculopathy or glaucoma which require monitoring with optical coherence tomography (OCT). Since OCT is a light-based test and changes the refractive status of the eye (in the cornea or the lens), it can potentially affect the results of the OCT measurements but has not been sufficiently studied. This pilot study aims at studying the potential change in OCT parameters in the eye after undergoing such surgery.

Detailed description

Refractive surgeries are widely used in patients with ametropia. Refractive surgery is most commonly performed in patients with myopia. These patients often have a predilection for developing other conditions in the posterior segment of the eye, like myopic maculopathy or glaucoma which require monitoring with optical coherence tomography (OCT). Since OCT is a light-based test and changes in the refractive status of the eye (in the cornea or the lens) can potentially affect the results of the OCT measurements. Literature review reveals that the effect of significant changes in refractive power of the eye on the parameters of optical coherence tomography (OCT) has not been sufficiently studied. Some authors simulated the effect of refractive surgery using a contact lens but had diverging results. This prospective pilot study aims at studying the potential change in OCT parameters in the eye after undergoing refractive surgery.

Interventions

DIAGNOSTIC_TESTOptical coherence tomography

Posterior segment OCT (a non-contact procedure performed over one minute) is additionally performed for patients participating in this study. Proportion of change in measurements in microns will be analyzed.

Sponsors

University of Nebraska
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patients undergoing refractive surgery 2. For patients undergoing bilateral eye surgery, the one with higher degree of ametropia will be included.

Exclusion criteria

1. Astigmatism more than 3 Diopters 2. Visual acuity worse than 20/25 3. Patients with unstable visual fixation 4. Severe Dry Eye

Design outcomes

Primary

MeasureTime frameDescription
Macular thickness1 day after refractive procedureProportion of Change in thickness of retina and its layers measured in microns

Secondary

MeasureTime frameDescription
Choroidal thickness1 day after refractive procedureProportion of Change in thickness of choroid and its layers measured in microns
visual acuity1 day after refractive procedureProportion of Change in clarity of vision, measured in logarithm of Minimal Angle of Resolution (logMAR) units
central corneal thickness1 day after refractive procedureProportion of Change in thickness of cornea measured in microns
anterior chamber depth1 day after refractive procedureProportion of Change in depth of anterior chamber of the eye measured in microns
keratometry1 day after refractive procedureProportion of Change in corneal curvature measured in diopters

Countries

United States

Contacts

CONTACTPukhraj P Rishi, MBBS
pukhraj.rishi@unmc.edu402-559-2020
CONTACTLisa Reid
lisa.reid@unmc.edu4025591851
PRINCIPAL_INVESTIGATORPukhraj P Rishi, MBBS

University of Nebraska

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 27, 2026