To evaluate the human eye irritation potential of two test sunscreen formulation
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
TRIPLE
Enrollment
48
Study staff will administer the control in one eye and a test sunscreen in the other eye according to the assigned randomization schedule.
Study staff will administer the control in one eye and a test sunscreen in the other eye according to the assigned randomization schedule.
Study staff will administer the control in one eye and a test sunscreen in the other eye according to the assigned randomization schedule.
Unnamed facility
St. Petersburg, Florida, United States
Subjective assessment of discomfort in the eyes assessed by 5 point scale
Time frame: Up to 1 day
Intensity of Lacrimation assessed by 5 grading scale
Time frame: Up to 1 day
Intensity of Bulbar Conjunctiva Irritation assessed by 4 grading scale
Time frame: Up to 1 day
Intensity of Palpebral Conjunctiva Irritation assessed by 4 grading scale
Time frame: Up to 1 day
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