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Repeatability and reproducibility of corneal epithelial thickness mapping and its application for screening in refractive surgery

Conditions
Corneal refractive surgery
Registration Number
DRKS00032797
Lead Sponsor
Promoter's representative of OFTALVIST (Oftalmología Vistahermosa, SL)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
64
Inclusion Criteria

1. Written informed consent for participation in the study and data protection.
2. Individuals looking for corneal refractive surgery with and without corneal alterations.
3. No active ocular disease (other than the target condition).

Exclusion Criteria

1. Subjects who had a history of corneal surgery or any other major ocular surgery.
2. Use of soft contact lens within two weeks prior to measurements, or use of rigid gas permeable contact lens within four weeks after measurements.
3. Subjects unable to set and follow instructions (inability to comply with imaging protocol).
4. Pregnancy or lactancy.

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The aim of this study is to evaluate the repeatability and reproducibility of EEC mapping with CIRRUS 5000 OCT equipment in patients coming to the center for corneal refractive surgery.
Secondary Outcome Measures
NameTimeMethod
To investigate the usefulness of the CIRRUS 5000 OCT equipment in determining patient eligibility for corneal refractive surgery.
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