Objective: To evaluate the efficiency of nano-formulating dexamethasone in the
treatment of anterior uveitis. Methods: The present study is a randomized
clinical trial study conducted on 20 patients with anterior uveitis referred to
the Ophthalmology Department of Imam Khomeini Hospital, Ahvaz
University of Medical Science from June 2019 to March 2020. Patients were
divided into two groups randomly with 10 subjects in each group. One group
of patients received micellar nanoparticle containing 0.1% dexamethasone
(DEX) (the nanoparticle group) and another group received 0.1% DEX
solution (the control group). In the 1st, 3rd, 7th, 14th, and 28th day of the
treatment and second month after treatment, the patients were followed-up
clinically. The number of visible cells in the anterior chamber are counted and
graded on a scale of 0 to 4 based on the Standardization of Uveitis
Nomenclature Working Group. Visual acuity, posterior adhesion, cell count of
anterior chamber, flare, hypopyon, and intraocular pressure was compared
between the two groups. Besides, the correlation between hypopyon and
vision, the cell count in the anterior chamber and visual acuity, visual acuity
and flare, visual acuity and posterior adhesion. Results: There was a difference
in visual acuity, removal of posterior adhesion, cell count of anterior chamber,
flare, improving hypopyon, intraocular pressure significantly between the
nano DEX group and the control group (P<0.05). Conclusions: The use of 0.1%
DEX nanoparticles can be quite effective in anterior uveitis treatment.
Therefore, more controlled studies are needed to understand and recognize
the effects of DEX nanoparticles in the treatment of uveitis.
Keywords: Uveitis; Nano-micellar compounds containing dexamethasone;
Flare; Hypopyon