iLux Treatment for Meibomian Gland Dysfunction (MGD)

Completed · Not applicable

Conditions studied: Evaporative Dry Eye

In brief

The purpose of this study is to assess changes in meibomian gland function and evaporative dry eye symptoms after treatment with the iLux medical device.

Key facts

Study ID

NCT03055650

Run by

Tear Film Innovations, Inc.

People needed

30

Starts

2015-12-07

Expected to finish

2016-02-18

Last updated by the study team

2020-11-12

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age 18 years and older of any gender or race
• Provision of written informed consent prior to study participation
• Willingness and ability to return for all study visits
• A positive history of self-reported dry eye symptoms for three months prior to the study using the Standard Patient Evaluation of Eye Dryness (SPEED) questionnaire, and a score of > 6.
• Need for regular use of artificial tears, lubricants, or rewetting drops in both eyes
• Evidence of meibomian gland (MG) obstruction, based on a total meibomian gland secretion score of < 12 out of a maximum score of 45, for 15 glands (5 nasal, 5 medial, 5 temporal) of the lower eyelid of each eye. Glands expressed \& graded from 0 to 3 (0 = no secretion, 1 = inspissated, 2 = cloudy, 3 = clear liquid).

You may not qualify if…

• History of ocular surgery including intraocular, oculo-plastic, corneal or refractive surgery within 1 year
• Ocular trauma or herpetic keratitis within the previous 3 months
• Cicatricial lid margin disease identified via slit lamp examination, including pemphigoid, symblepharon, etc.
• Active ocular infection (e.g., viral, bacterial, mycobacterial, protozoan, or fungal infection of the cornea, conjunctiva, lacrimal gland, lacrimal sac, or eyelids including a hordeolum or stye)
• Active ocular inflammation or history of chronic, recurrent ocular inflammation within prior 3 months (e.g. retinitis, macular inflammation, choroiditis, uveitis, iritis, scleritis, episcleritis, keratitis)
• Ocular surface abnormality that may compromise corneal integrity (e.g., prior chemical burn, recurrent corneal erosion, corneal epithelial defect, Grade 3 corneal fluorescein staining, or map dot fingerprint dystrophy
• Lid surface abnormalities (e.g., entropion, ectropion, tumor, edema, blepharospasm, lagophthalmos, severe trichiasis, severe ptosis) that affect lid function in either eye
• Anterior blepharitis (staphylococcal, demodex or seborrheic grade 3 or 4)
• Ocular trauma, chemical burns, or limbal stem cell deficiency
• Systemic disease conditions that cause dry eye (e.g., Stevens-Johnson syndrome, vitamin A deficiency, rheumatoid arthritis, Wegener's granulomatosis, sarcoidosis, leukemia, Riley-Day syndrome, systemic lupus erythematosus, Sjogren's syndrome)
• Women who are pregnant, nursing, or not utilizing adequate birth control measures
• Individuals who have either changed the dosing of systemic or ophthalmic medication within the past 30 days prior to screening or who are unable or unwilling to remain on a stable dosing regimen for the duration of the study
• Individuals using isotretinoin (Accutane) within 1 year, cyclosporine-A (Restasis) within 2 months, or topical medications other than non-preserved artificial tears within 2 weeks.
• Individuals using another investigational device or agent within 30 days of study participation
• Contact lens wearers or individuals who have worn contact lenses in the last 30 days or anticipate wearing contact lenses during this study.

Where it is running

• TearFilm Investigative Site — Encinitas, California, United States
• TearFilm Investigative Site — San Diego, California, United States
• TearFilm Investigative Site — San Diego, California, United States

Full record on ClinicalTrials.gov

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