Evaluation of Corneal Epithelial Mapping in Diagnosis of Early Keratoconus by Anterior Segment Optical Coherence Tomography
NCT ID: NCT06914973
Last Updated: 2025-04-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
150 participants
OBSERVATIONAL
2025-05-01
2026-08-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
High-resolution imaging of the cornea with AS-OCT provides thickness measurements individually for epithelium and stroma individually. Measuring corneal epithelial thickness adds information that could be of value in early diagnosis, progression evaluation and maybe even for a more complete understanding of the pathophysiology of this disease. It has been shown that changes in the corneal epithelial thickness could be a sensitive tool for early keratoconus detection as well as for the assessment of the disease progression.
Precise measurements of the epithelial thickness are therefore important for keratoconus diagnosis and follow-up. AS-OCTs have high axial resolution and studies have shown that these instruments provide repeatable epithelial measurements both in central and peripheral cornea. With an additional lens (anterior segment module), posterior segments OCTs can also be used to measure corneal parameters including epithelial thickness1and previous studies have shown that these modules can also produce precise epithelial thickness measurements in healthy corneas and in keratoconus. There is only limited information on how the precision of epithelial measurements with the anterior module in posterior segment OCTs compares to the precision of epithelial measurements with AS-OCTs Aim of this study Detect early-stage keratoconus by identifying suitable epithelial thickness changes before topographic abnormalities appear .
\- Provide higher accuracy compared to traditional topography by offering high-resolution cross-sectional imaging
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Correlation Between Eye Rubbing and Keratoconus Severity in a Treatment-naive Keratoconic Population
NCT02883881
Predicting Manifest Astigmatism in Keratoconus Patients.
NCT06798779
Correlation of Angle Kappa , Corneal High Order Aberrations and Total Eye Aberrations in Various Refractive Errors
NCT05741190
Reliability of Topography Measurements in Keratoconus
NCT03511495
Long-term Safety and Effectiveness of LASIK-Xtra Compared to Conventional LASIK
NCT06857032
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Group I
Control Group who intended to do LASIK (N=50)
No interventions assigned to this group
Group II
Keratoconus Group (N=50)
No interventions assigned to this group
Group III
Suspicious keratoconus by pentacam ( N=50)
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Keratoconus patients with a confirmed diagnosis (based on corneal topography, tomography, and clinical signs).
* Suspicious Keratoconus patients by pentacam.
* Age ≥ 18 years.
* Willingness to provide informed consent.
Exclusion Criteria
* Active ocular infection or inflammation.
* Severe dry eye disease or other conditions affecting corneal epithelium.
* Inability to cooperate with imaging procedures.
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Assiut University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Asmaa Refaat Nagib
residant doctor
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
mapping keratoconus OCT
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.