This phase I trial will assess primarily the safety and secondarily anti-inflammatory effect of Episcleral Dexamethasone in patients suffering from macular edema and other disorders of the retina, choroid and vitreous.
This phase I trial will assess primarily the safety and secondarily anti-inflammatory effect of Episcleral Dexamethasone in patients suffering from macular edema and other disorders of the retina, choroid and vitreous. Numerous studies have documented the anti-inflammatory activity of Dexamethasone in macular edema associated with diabetes, branch retinal vein occlusion, and non-infectious posterior uveitis. The investigators hypothesize that Episcleral Dexamethasone is safe, tolerable and that its anti-inflammatory activity will interface with the pro-inflammatory cascade associated with macular edema due to diabetes, surgery, trauma, vein occlusions, uveitis and retinal degeneration to improve visual structure and function. The investigators hypothesize that Episcleral Dexamethasone is safe, tolerable and that its anti-inflammatory activity will reduce macular edema and improve vision. The investigator's objective is to primarily assess the safety, tolerability and pharmacokinetics of Episcleral Dexamethasone in patients with macular edema; to secondarily assess efficacy in reducing macular edema and improving visual structure and function. The main outcome of the study is safety assessment. Secondary outcomes are assessment of visual acuity and anatomical changes in the macula as measured via optical coherence tomography (OCT) and fluorescein angiogram.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
2
Sustained Release Episcleral Dexamethasone
Stanford Medicine Ophthalmology
Palo Alto, California, United States
A primary outcome measure of the study is ocular safety assessment as measured by comprehensive ophthalmic exam.
Assessment of ocular safety as measured by comprehensive ophthalmic exam.
Time frame: 12 Months
A secondary outcome is assessment of visual acuity.
Secondary outcome is assessment of visual acuity.
Time frame: 12 Months
A secondary outcome is assessment of anatomical changes in the macula as measured via optical coherence tomography (OCT).
A secondary outcome is assessment of anatomical changes in the macula as measured via optical coherence tomography (OCT).
Time frame: 12 Months
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