To evaluate the human eye irritation potential of one test sunscreen formulation.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
TRIPLE
Enrollment
24
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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