Purpose: To determine the impact of short-term 4mg/ml dexamethasone solution treatment in diabetic macular edema (DME). Design: Phase II, randomized, prospective, parallel, interventional study. Participants: Pseudophakic patients with central-involved DME. Methods: Twenty-seven patients with visual impairment caused by DME were randomized in a 1:1:1 ratio, in order to investigate treatment with 0.01 ml, 0.03 ml and 0.05 ml intravitreous dexamethasone solutions, and followed-up over 28 days Outcome Measures: The primary outcome was macular thickness at three days after intravitreous dexamethasone. The secondary outcomes were macular thickness at 28 days after intravitreous dexamethasone, best-corrected visual acuity (BCVA) and intraocular pressure (IOP) at three and 28 days after intravitreous dexamethasone
This is a prospective, phase II, randomized, interventional, monocentric study. Data of consecutive patients with DME who volunteered to participate in the research at the department of ophthalmology of State University of Campinas (UNICAMP) - Brazil between May 2016 and December 2017 were analysed. At the screening visit, all patients underwent complete ophthalmic evaluation, including best corrected visual acuity (BCVA), slit-lamp biomicroscopy, applanation tonometry, fundus biomicroscopy, fluorescein angiography (Visucam NM/ FA Carl Zeiss; Carl Zeiss Meditec, California, USA), SD- OCT (Spectralis; Heidelberg Engineering, Heidelberg, Germany). Central macular thickness was obtained through 7 horizontal lines ( 30° x 5° area), centered on the fovea, with 1536 A scans per line at 240 µm intervals. At the baseline study visit, patients were randomized with a 1:1:1 allocation to receive dexamethasone solution 4 mg/ml: 0,01 ml (40 µg) ; or 0,03 ml (120 µg); or 0,05 ml (200 µg). In follow up visits (1, 3, 7, 14, 21, 28 days after) were performed BCVA, slit-lamp biomicroscopy, applanation tonometry, fundus biomicroscopy, SD- OCT.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
27
0,01 ml intravitreous dexamethasone solution 4mg/ml injection.
0,03 ml intravitreous dexamethasone solution 4mg/ml injection.
0,05 ml intravitreous dexamethasone solution 4mg/ml injection.
State University of Campinas
Campinas, São Paulo, Brazil
Macular Thickness at 3 Days After Intravitreous Dexamethasone
Measure macular thickness at 3 days after intravitreous dexamethasone with OCT - unit µm
Time frame: Three days after intravitreous dexamethasone
Macular Thickness at 28 Days After Intravitreous Dexamethasone
Measure macular thickness at 28 days after intravitreous dexamethasone with OCT - unit µm
Time frame: 28 days after intravitreous dexamethasone
Best Corrected Visual Acuity (BCVA) at 3 Days After Intravitreous Dexamethasone
Measure best corrected visual acuity (BCVA) at 3 days after intravitreous dexamethasone with ETDRS chart
Time frame: Three days after intravitreous dexamethasone
Best Corrected Visual Acuity (BCVA) at 28 Days After Intravitreous Dexamethasone
Measure best corrected visual acuity (BCVA) at 28 days after intravitreous dexamethasone with ETDRS chart
Time frame: 28 days after intravitreous dexamethasone
Intraocular Pressure (IOP) at 3 Days After Intravitreous Dexamethasone
Measure intraocular pressure (IOP) 3 days after intravitreous dexamethasone - unit mmHg
Time frame: 3 days after intravitreous dexamethasone
Intraocular Pressure (IOP) at 28 Days After Intravitreous Dexamethasone
Measure intraocular pressure (IOP) 28 days intravitreous dexamethasone - unit mmHg
Time frame: 28 days after intravitreous dexamethasone
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