Corneal Elastography and Patient Specific Modeling

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age16-80
SponsorThe Cleveland Clinic

About this trial

The goal of this research is to develop measurement tools and simulation technology for characterizing and predicting individual responses to corneal treatments and for advancing understanding of corneal ectasia risk factors. Patients who either 1) have keratoconus and are being evaluated for corneal crosslinking or 2) have refractive error and are being evaluated for refractive surgery procedures such as LASIK will have their eyes imaged to assess their mechanical properties and will have computational simulations performed to predict the response to treatment. One aim of the study is to test the hypothesis that computational models can predict the cornea's shape changes within clinically acceptable limits of error.

Eligibility criteria

Qualifiers

Any patient with keratoconus diagnosed by standard criteria, including topographic steepness, irregular astigmatism with a pattern consistent with keratoconus.

Any patient deemed a candidate for LASIK (laser vision correction) and scheduled for surgery.

Disqualifiers

Inability to provide informed consent, including non-English speaking (if interpreter not available) and cognitively/mentally impaired (if legal guardian not available).

Trial design

Treatments tested in this trial

  • Optical coherence tomography

Treatment groups

No treatment groups listed

Locations

1
Cleveland Clinic Foundation Cole Eye Institute44195, ClevelandOhio, United States

Sponsors and collaborators

The Cleveland Clinic

Lead sponsor