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MyopiaNCT07647146

Corneal Epithelial Thickness Mapping by Anterior Segment Optical Coherence Tomography in Patients With Refractive Errors

An observational study of Myopia and Hyperopia, run by Sohag University at 1 site in Egypt.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record

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Trial summary

This study evaluates corneal epithelial thickness using anterior segment optical coherence tomography (AS-OCT) in patients with refractive errors. It aims to assess the relationship between epithelial thickness patterns and different types of refractive errors. Read more about this study

Who is it for?
Ages 18 to 99 yearsHealthy volunteers can take part
Conditions the study is for
Myopia, Hyperopia, Astigmatism
How many people
360 participants
Where
1 siteEgypt
Study dates
1 Jul 2026to 1 May 2027
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 99 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: Adult participants (≥18 years) with refractive errors, including myopia, hyperopia, and astigmatism, as well as emmetropic subjects, recruited from the Ophthalmology Department and undergoing anterior segment optical coherence tomography (AS-OCT) examination.

Who may be able to join

  • Age ≥ 18 years-
  • Patients diagnosed with myopia or hyperopia by refraction
  • Clear cornea with no evidence of corneal pathology
  • Ability to undergo reliable anterior segment imaging

Who cannot join

  • Inability to fixate or follow instructions
  • Family history of keratoconus
  • Glaucoma,Cataract
  • Previous ocular surgery including refractive surgery
  • Keratoconus or suspected corneal ectasia
  • Corneal opacities or scars
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  • Contact lens wear within the last two weeks
  • Ocular trauma
  • systemic disease affecting the cornea ( Such as diabetes)

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Merna romany loza, MBBCh, Ophthalmology Resident contact

01275800331

mernaromany54@yahoo.com

Engy Mohamed Mostafa, Professor contact

01005643587

Engymostafa@yahoo.com

Egypt1 site
  • Sohag University Hospital

    Sohag, Sohag Governorate, 82524

    Engy Mohamed Mostafa, Professor, 01005643587, Engymostafa@yahoo.com

    Amin Abu-Ali Hassan, Assistant Professor, 01015437008

Other trials in Egypt

About this study

This study evaluates corneal epithelial thickness using anterior segment optical coherence tomography (AS-OCT) in patients with refractive errors. It aims to assess the relationship between epithelial thickness patterns and different types of refractive errors.

Read the detailed description

Refractive errors are among the most common ocular conditions affecting visual acuity. Corneal epithelial thickness has been suggested to play a role in the optical properties of the eye and may vary among different refractive states. This observational study aims to evaluate corneal epithelial thickness mapping using anterior segment optical coherence tomography (AS-OCT) in patients with refractive errors. Patients will be assessed and categorized according to their refractive status, and epithelial thickness measurements will be obtained and analyzed. The study seeks to investigate potential correlations between epithelial thickness distribution and different types of refractive errors to enhance understanding of corneal biomechanics in refractive conditions.

Keywords
Corneal epithelial thickness, AS-OCT, anterior segment optical coherence tomography, refractive errors, myopia, hyperopia, astigmatism, cornea
Medical subject headings
Myopia, Hyperopia, Astigmatism, Refractive Errors, Corneal Diseases

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07647146
Study groupRoleWhat they receive
All ParticipantsAll participants diagnosed with refractive errors (myopia, hyperopia, astigmatism) and emmetropia will be included in the study. All subjects will undergo anterior segment optical coherence tomography (AS-OCT) for corneal epithelial thickness mapping. Participants will then be analyzed according to their refractive status.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Measurement of corneal epithelial thickness using AS-OCT

    Corneal epithelial thickness will be measured using anterior segment optical coherence tomography (AS-OCT). Measurements will include central and regional epithelial thickness values in microns in patients with different refractive errors.

    Measured: At baseline during a single study visit when participants undergo AS-OCT examination.

Secondary outcomes (4)
  1. Comparison of epithelial thickness between myopic and hyperopic eyes

    Corneal epithelial thickness will be compared between myopic and hyperopic eyes using AS-OCT measurements.

    Measured: At baseline (single visit)

  2. Comparison of epithelial thickness in eyes with and without astigmatism

    Corneal epithelial thickness will be evaluated and compared between eyes with astigmatism and those without astigmatism using AS-OCT.

    Measured: At baseline (single visit)

  3. Corneal epithelial thickness asymmetry across corneal regions and inter-eye comparison

    Epithelial thickness will be assessed across different corneal regions and compared between both eyes to evaluate inter-eye asymmetry.

    Measured: At baseline (single visit)

  4. Comparison of epithelial thickness in low and high refractive errors

    Corneal epithelial thickness profiles will be compared between low and high degrees of myopia and hyperopia using AS-OCT measurements.

    Measured: At baseline (single visit)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Jun 2026
  2. Study start1 Jul 2026 (estimated)
  3. Primary completion1 May 2027 (estimated)
  4. Study completion1 May 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
360 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07647146
Sponsor's protocol ID
Soh-Med-26-5-7MS
Status last verified
Jun 2026
First submitted
9 Jun 2026
Last updated
15 Jun 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Individual participant data will not be shared.

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