Allergic Conjunctivitis
Conditions
Brief summary
The purpose of this study is to evaluate the comfort of BEPREVE compared to LASTACAFT after instillation.
Detailed description
After one drop is instilled subjects will complete a comfort assessment at 1, 3, 5, and 10 minutes after drop instillation.
Interventions
None listed
Sponsors
Bausch & Lomb Incorporated
Cunningham, Derek N., O.D., P.A.
Study design
Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
Each patient must meet the following criteria to be enrolled in this study: 1. Are male or female at least 18 years of age who are diagnosed with allergic conjunctivitis. 2. Have allergic ocular symptoms within the last three days. 3. Are willing/able to follow instructions from the study investigator and his/her staff. 4. Have signed informed consent approved by Institutional Review Board or Independent Ethics Committee.
Exclusion criteria
Patients who meet any of the following criteria will be excluded from the study: 1. Have known hypersensitivity to either BEPREVE™ or LASTACAFT® or to any component of the test article (including procedural medications such as anesthetic and/or fluorescein drops, dilating drops, etc.). 2. Have active corneal pathology noted in the study eye at the screening visit. Active corneal pathology is defined as corneal pathology that is non stable, or greater than mild, or will compromise assessment of the safety or efficacy of treatment. 3. Are pregnant or nursing/lactating.
Countries
United States
Outcome results
None listed