Mucin Levels in Dry Eye and Normal Populations
Completed
Conditions studied: Dry Eye
In brief
The purpose of this study is to evaluate changes in ocular mucin levels in response to a drying environment in subjects with dry eye disease as well as patients who report no history of dry eye disease. It is expected that exposure to the dry environment will alter mucin levels in different ways when comparing the two groups.
Key facts
- Study ID
- NCT05911555
- Run by
- ORA, Inc.
- People needed
- 34
- Starts
- 2013-05-01
- Expected to finish
- 2013-05-01
- Last updated by the study team
- 2023-06-22
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Be male or female of any race, at least 18 years of age at Visit 1.
- Have provided verbal and written informed consent.
- Have a best corrected visual acuity of +0.70 logMAR or better in both eyes at Visit 1, as assessed by Early Treatment of Diabetic Retinopathy Study (ETDRS) chart.
- If a woman of childbearing potential, have a negative urine pregnancy test at Visit 1 and agree to use a medically acceptable form of birth control throughout the study duration . [Females are considered of childbearing potential unless they are surgically sterilized (bilateral tubal ligation, hysterectomy or bilateral oophorectomy) or post-menopausal (at least 12 months since last menses).]
- Have previously completed a recent trial OR not completed a recent trial AND report no symptoms of dry eye disease.
You may not qualify if…
- 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
Where it is running
- Andover Eye Associates — Andover, Massachusetts, United States
Full record on ClinicalTrials.gov
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