Effect of Controlled Adverse Environment (CAE) on Tear Film Stability
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Details and patient eligibility
About
The purpose of this study is to evaluate the effect of the controlled adverse environment (CAE) on Mean Break-Up Area in subjects diagnosed with Dry Eye Syndrome.
Full description
Single-Center, Pilot, controlled adverse environment (CAE) Study.
This is a single-center, one visit, pilot, CAE study. Dry Eye Subjects (N=30) who qualify will undergo tear film video recording, fluorescein staining, and break up time before CAE exposure and after CAE exposure.
All subjects will undergo baseline dry eye assessments including fluorescein staining, breakup time, conjunctival redness and tear film video recording. Subjects who qualify will then undergo CAE exposure for 90 minutes. At the end of CAE exposure subjects will undergo dry eye assessments again.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
- At least 18 years of age & either sex, any race
- Willing and able to follow all instructions
- Positive history of dry eye disease
- Use or desire to use drops for dry eye within the past 6 months
Exclusion criteria
- Have planned surgery during trial period
- Female currently pregnant, planning a pregnancy or lactating
- Use of disallowed medications
- Have ocular infections, or ocular conditions that could affect study parameters
- Have used an investigational drug or device within 30 days of start of study
- Female that is currently pregnant, planning a pregnancy or lactating
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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