The purpose of this research is to measure daytime open-eye response to wearing of narafilcon B lenses.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
22
Coles-Brennan Pty Ltd
Hawthorn, Victoria, Australia
Corneal Thickness
Percentage of corneal swelling (positive value) or deswelling (negative value) measured with Haag-Streit pachymetry equipment in microns, reported as a percent.
Time frame: After 8 hours of contact lens wear
Endothelial Blebs
Corneal images captured with equipment are measured, manually outlined to estimate total bleb area from 0 to 100%. This is measured as a change in percentage after 20 minutes compared to the value prior to lens wear (baseline).
Time frame: baseline, after 20 minutes of treatment conditions
Limbal Redness
Scale of 0 to 4, where 0=none and 4= severe redness. Measure reported as a comparison of 8 hours of wear to baseline with the difference being reported.
Time frame: Baseline, After 8 hours of treatment conditions
Overall Comfort
Patient reported subjective comfort of lenses or spectacles (range 0-100, where 100 is best).
Time frame: after 8 hours
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None - subject used own spectacles