Corneal refractive surgery
Conditions
Interventions
Group 1: All patients participating in the study will undergo corneal refractive surgery and will be measured with the CIRRUS 5000 OCT equipment. All patients will be treated according to standard cl
Sponsors
Promoter's representative of OFTALVIST (Oftalmología Vistahermosa, SL)
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
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
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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| To investigate the usefulness of the CIRRUS 5000 OCT equipment in determining patient eligibility for corneal refractive surgery. | — |
Countries
Spain
Contacts
Public ContactMaria Cobo
OFTALVIST
Outcome results
None listed