Evaluation of the Stinging Potential of Products in Human Eyes

Completed · Not applicable · Has a placebo group

Conditions studied: Sunscreen Agents

In brief

The objective of this study was to compare the human eye stinging potential of experimental formulas and an industry standard shampoo mixture. The study was conducted under the supervision of a Board Certified Ophthalmologist. The study design was a three cell, single blind study. Subjects were given the industry standard shampoo mixture in one eye and an exploratory sunscreen in the other as according to the randomization schedule.

Key facts

Study ID

NCT02872194

Run by

Bayer

People needed

21

Starts

2014-09-05

Expected to finish

2014-09-06

Last updated by the study team

2018-12-12

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Male or female subjects, aged 18 to 65 years
• No medical conditions of the eyes as determined by the subjects' medical history and confirmed by ophthalmologist
• Subjects do not wear contact lenses or, if he/she does wear contact lenses, is willing to refrain from wearing these during the day of and day after the study
• Subject is willing to have the test materials instilled into the eyes and follow all protocol requirements
• Subject is willing to refrain from using false eyelashes of any type or any topical prescription, OTC or cosmetic products on their eyes, eyelids, eyelashes or the peri-orbital areas of the face on the day of the study.
• Subjects should refrain from use of make-up on testing day

Where it is running

• Study site — St. Petersburg, Florida, United States

Full record on ClinicalTrials.gov

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