Efficacy of Topical Cyclosporin for Ocular Rosacea
Completed · Phase 4
Conditions studied: Rosacea
In brief
The purpose of this study is to determine whether Restasis (topical cyclosporin) is effective in the treatment of ocular rosacea
Key facts
- Study ID
- NCT00348335
- Run by
- Ophthalmic Consultants of Long Island
- People needed
- 35
- Starts
- 2006-06-01
- Expected to finish
- 2007-09-01
- Last updated by the study team
- 2011-07-29
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Patient at least 18 years old, but younger than 65
- Diagnosis of acne rosacea
- Active ocular rosacea based on lid findings of meibomian gland dysfunction with lid telangiectasia and hyperemia of at least 2+
- Schirmers test of greater than 5mm in at least 1 eye
- If patient currently using lid hygiene must maintain regimen during study
- Stop oral antibiotics at least 4 weeks prior
You may not qualify if…
- Use of topical cyclosporin within last 90 days
- Visual acuity of 20/100 or better in both eyes
- Pregnant or lactating females
- Active ocular infection
- Scarring of central cornea
- Eyelid defects,abnormal lid positioning or lagophthalmos
- Flax seed or Fish oil supplements within last 30 days
Where it is running
- 2500 Rte 347 Bldg 24 — Stony Brook, New York, United States
Full record on ClinicalTrials.gov
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