Trials / Completed
CompletedNCT01339507
A Patient Reported Ocular Comfort Assessment Comparing Bepreve to Lastacaft
A Patient Reported Ocular Comfort Assessment Comparing Bepreve to Lastacaft in Patients With a History of Allergic Conjunctivitis
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 25 (actual)
- Sponsor
- Cunningham, Derek N., O.D., P.A. · Individual
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
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.
Conditions
Timeline
- Start date
- 2011-04-01
- Primary completion
- 2011-05-01
- Completion
- 2011-06-01
- First posted
- 2011-04-20
- Last updated
- 2016-01-27
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01339507. Inclusion in this directory is not an endorsement.