The Efficacy of an Ocular Emulsion in Meibomian Gland Dysfunction
Completed · Not applicable
Conditions studied: Meibomian Gland Dysfunction
In brief
The aim of this study will be to determine the efficacy of this novel, lipid-containing artificial tear on the signs and symptoms of meibomian gland disease.
Key facts
- Study ID
- NCT01207752
- Run by
- Southern California College of Optometry at Marshall B. Ketchum University
- People needed
- 69
- Starts
- 2010-09-01
- Expected to finish
- 2011-07-01
- Last updated by the study team
- 2025-04-01
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Schein symptom score (all 6 questions) of greater than 5,
- evidence of MGD changes in both eyes (i.e.,
- lower eyelid secretion quality score greater than 1.0 (0 - 3 scale) OR gland dropout score greater than 1.0 (i.e., greater than 25% of entire lower eyelid) as demonstrated by meiboscopy, and corneal staining of grade 4.0 or greater (0 - 20 scale).
You may not qualify if…
- contact lens wear, use of topical ocular medication other than artificial tears (use of Restasis is specifically excluded),
- unstable systemic medication use (i.e., anti-histamines, steroids, etc.), recent (within 6 months of study start) ocular trauma or surgery,
- diabetes, aqueous deficient dry eye (defined as a Schirmer I value (without anesthetic) of < 5 mm of wetting in 5 minutes in either eye), and use of punctal plugs.
- Subjects taking omega 3 fatty acid supplements for dry eye can be included so long as their intake is stable for the prior six months and they meet the inclusion criteria above. -
Where it is running
- Eye Care Center — Fullerton, California, United States
Full record on ClinicalTrials.gov
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