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Chromatic and Monochromatic Optical Aberrations After Corneal Refractive Surgery

Chromatic and Monochromatic Optical Aberrations After Corneal Refractive Surgery - Preliminary Study Assessing Their Prevalence, Methods of Reductions of Symptoms and Time-dependent Changes in Patients Symptoms

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03893838
Enrollment
100
Registered
2019-03-28
Start date
2019-02-01
Completion date
2024-02-01
Last updated
2022-03-29

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

Conditions

Aberration, Corneal Wavefront, Refractive Errors

Brief summary

Refractive surgeries can be divided into two distinct categories: 1) corneal surgeries (superficial and deep procedures) carried on the surface of the eye and 2) lens surgeries (phakic IOL, refractive lens exchange) - an intraocular intervention, performed in the anterior or posterior chamber or on the lens. In the proposed protocol focus is on the corneal refractive surgeries impact on monochromatic higher-order aberrations on the one hand and chromatic aberrations on the other. During the surgery in order to get the patient emmetropic, refractive surgery corrects optical defects by decreasing aberrations of lower orders ) simultaneously increases high-order aberrations (that is perceived by the patient as halo, glare or starburst). Informations about prevalence and causes of higher order aberrations after refractive surgery are numerous but there is no information about chromatic aberrations.

Interventions

None listed

Sponsors

Wroclaw Medical University
CollaboratorOTHER
Wrocław University of Science and Technology
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* patient after corneal refractive surgery at least for 4 months * post surgical refraction within +/- 0.75 diopter of spherical and +/- 1.0 diopter of cylindrical error * willing and able to understand and sign an informed consent form.

Exclusion criteria

* patient unable to participate in the study * any corneal diseases, eyes trauma or systemic diseases history; keratoconus or tendency of keratoconus * corneal macula and obvious pannus; current enrolment in another clinical trial/research project

Design outcomes

Primary

MeasureTime frameDescription
Chromoretinoscopy for near (MEM) and distance6 monthsConducted with a modified by researchers retinoscopy with distinct filters
Aberrometry reading for corneal HOA6 monthsConducted with aberrometer and corneal tomography
Transverse chromatic aberration6 monthsConducted with a modified by researchers aniseikonia test (with red and green lenses)
number of high order and chromatic aberrations after refractive surgery6 monthsnumber of high order and chromatic aberrations after refractive surgery

Secondary

MeasureTime frameDescription
Change of contrast sensitivity for near vision6 monthswithout and after the introduction of glasses with accommodation support, a blue light filter or concave lenses up to -0,5 diopter
Visual Function Questionaire 256 monthsConducted with VFQ-25 test
Change in Hue 100 test6 monthswithout and after the introduction of glasses with accommodation support, a blue light filter or concave lenses up to -0,5 diopter

Countries

Poland

Outcome results

None listed

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