Z01.0
Conditions
Interventions
Group 1: The first eye of enrolled subjects shall be measured once with the SMRT device before the Laser treatment.
Sponsors
OptiMedica Corporation
Eligibility
Sex/Gender
All
Age
22 Years to No maximum
Inclusion criteria
Inclusion criteria: *Male or female at least 22 years of age at the time of preoperative examination *At least 0.5 D of corneal cylinder *Clear intraocular media, except for the presence of cataract *Willing and able to participate in the study *Able to fixate *Signed informed consent
Exclusion criteria
Exclusion criteria: *History of prior intraocular or corneal surgery, active ophthalmic disease, or other ocular abnormality in the study eye(s), which in the opinion of the investigator would confound the study results. *Evidence of keratoconus or abnormal topography in the study eye(s), which in the opinion of the investigator would confound the study results. *Patient is pregnant, plans to become pregnant, is lactating or has another condition associated with the fluctuation of hormones that could lead to refractive changes *Concurrent participation or participation within 30 days prior to preoperative visit in any other clinical trial
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| SMRT measurement success rate | — |
Countries
Austria, Germany
Contacts
Public ContactMichael Faust
AMO Germany GmbH
Outcome results
None listed