Glaucoma Clinical Trial
Official title:
In Vivo Effects of Antiglaucomatous Prostaglandin Therapy on Immune Cells, Epithelium, and Nerves of the Ocular Surface: A Laser In Vivo Confocal Microscopy Study
The purpose of the study is to compare the efficacy of FDA-approved Travoprost (Travatan Z)
and Latanoprost (Xalatan)as anti-glaucoma treatment. Several studies indicate that glaucoma
medications may be associated with decreased tear production and tear film break-up time
(TBUT), and increased inflammatory cells in the conjunctiva (membrane lining of the eye lids
and the covering of the eye) leading to dry eye. Normal tear film (coating of the eye) is
continuous and blinking maintains the tear film continuity. If you keep your eyes open long
enough without blinking, the tear film will start breaking up. Your eye will feel
uncomfortable forcing you to blink. In patients with dry eyes, the tear film is unstable,
and breaks up faster. Therefore the tear break up time in patients who have dry eyes is
shorter.
In this study, the investigators will be comparing the two previously mentioned FDA-approved
eye drops Latanoprost and Travoprost. The difference between the two medications is a
preservative called benzalkonium chloride (BAK). Latanoprost contains BAK while Travoprost
does not. The investigators will be comparing the efficacy of each medication in lowering
IOP as well as trying to track the density of immune cells across the corneal surface by
taking photos of your eye. The investigators will also be assessing whether either drop
leads to symptoms of dry eye by comparing results from ocular surface exam tests such as
TBUT.
The purpose of the study is to compare the early effects of two anti-glaucoma eye drops on
eye pressure and inflammation of the eye using a microscope. One of the eye drops contains a
commonly used preservative, benzalkonium chloride (BAK), while the other is free of this
preservative, instead it utilises a new ionic buffer system called SofZia. Prolonged use of
BAK may be damaging to the eye surface and thus being investigated at a microscopic level in
this study.
Specific aims are to assess the in vivo effect of topical BAK-containing and BAK-free
prostaglandin analogue anti-glaucoma therapy on intraocular pressure (IOP), as well as on
density and morphology of corneal immune cells, epithelial cells and sub-basal nerve plexus.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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