This prospective, open-label, single-center, randomized, investigator-sponsored clinical study seeks to compare patient-reported and clinical outcomes with DEXTENZA versus topical steroid or antihistamine treatment in patients with allergic conjunctivitis
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
31
Dextenza 0.4Mg Ophthalmic Insert
0.2% loteprednol etabonate ophthalmic suspension
olopatadine hydrochloride ophthalmic solution 0.7%
Clinical Research Center of Florida
Pompano Beach, Florida, United States
Patient-reported treatment preference of self-administered topical therapy versus physician-administered therapy at Day 30 (final visit)
Patient-reported treatment preference of self-administered topical therapy versus physician-administered therapy at Day 30 (final visit)
Time frame: 30 days
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