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Study identifier: NCT04910503 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Medico Economic Evaluation of Fluocinolone Acetonide Implant Versus Dexametheasone Implant in Resistant Diabetic Macular Oedema

Condition: Diabetic Macular Edema  ·  Sponsor: Centre Hospitalier Universitaire Dijon

PhasePhase 4
Planned participants106
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Diabetic macular oedema (DME) is the main cause of visual impairment (or visual acuity) in patients with diabetic retinopathy, as it leads to progressive thickening of the retina, which in the long term leads to progressive death of the photoreceptor cells. It is therefore important to continue to treat macular oedema that has been progressing for several months or even years (resistant DME). The management of DME necessarily involves controlling diabetes (improving glycated haemoglobin levels) and blood pressure, but this is often not enough. Thus, when DME is significant and leads to a decrease in visual acuity, treatments are administered directly into the eye (intravitreal injections). For some years now, corticosteroids have been injected into the vitreous body (the gel that fills the eyeball) through the white of the eye for their anti-inflammatory properties. Indeed, these drugs improve the permeability of the retinal vessels and thus reduce oedema. These intravitreal implants are most often used in patients who have already undergone cataract surgery (pseudophakic) because corticosteroids also tend to aggravate a cataract. Currently, there are two implants containing corticosteroids that can be injected: the dexamethasone implant and the fluocinolone acetonide implant. These two implants have different properties, particularly with regard to their duration of action. Today, the overall management at 3 years and the quality of life associated with the treatments des…

This description comes directly from the study's public registry record.

Talk to the study team

Catherine CREUZOT-GARCHER  ·  03.80.29.51.73  ·  catherine.creuzot-garcher@chu-dijon.fr

Always discuss trial participation with your own doctor first.

Locations (1)

CHU Dijon-BourgogneDijon, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT04910503