This is a prospective clinical study that will be conducted at one clinical site located in the United States to assess anterior segment parameters with the ANTERION
Study Type
OBSERVATIONAL
Enrollment
176
3 repeat measurements performed with two of the ANTERION acquisition types and 3 repeat measurements performed with 2 acquisition types of the references devices
State University of New York College of Optometry
New York, New York, United States
Precision and Agreement 1
Reproducibility, repeatability and agreement of Anterior Corneal Topography parameters (3mm ring) of ANTERION and the reference device
Time frame: 1 day
Precision and Agreement 2
Reproducibility, repeatability and agreement of Anterior Corneal Topography parameters (6mm zone) of ANTERION and the reference device
Time frame: 1 day
Precision and Agreement 3
Reproducibility, repeatability and agreement of Posterior Corneal Topography parameters (3mm ring) of ANTERION and the reference device
Time frame: 1 day
Precision and Agreement 4
Reproducibility, repeatability and agreement of Posterior Corneal Topography parameters (6mm zone) of ANTERION and the reference device
Time frame: 1 day
Precision and Agreement 5
Reproducibility, repeatability and agreement of Cornea Thickness (µm) of ANTERION and the reference device
Time frame: 1 day
Precision and Agreement 6
Reproducibility, repeatability and agreement of Lens Thickness, ACD, Pupil Diameter, White-to-White, Axial Length (mm) of ANTERION and the reference device
Time frame: 1 day
Precision and Agreement 7
Reproducibility, repeatability and agreement of Anterior Chamber Volume (mm\^3) of ANTERION and the reference device
Time frame: 1 day
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Adverse Events Rate
Adverse events found during the clinical study
Time frame: 1 day