The purpose of this study was to evaluate subject perceptions of Olopatadine 0.2%, dosed once-daily, in subjects with allergic conjunctivitis and to record any adverse events as described by the subjects as a part of this post marketing surveillance study.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
300
Olopatadine Hydrochloride Ophthalmic Solution, 0.2%, one drop once a day for one week
Unnamed facility
Kolkata, India
Overall Patient Satisfaction
As assessed by the subject on a questionnaire
Time frame: Day 7
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