Comparative Study of Dexamethasone Implant to Intravitreal Aflibercept in Subjects With Diabetic Macular Edema
Condition: Diabetic Macular Edema · Sponsor: The Cleveland Clinic
About this study
This study is an interventional, prospective randomized study comparing the dexamethasone implant to intravitreal aflibercept. Subjects will have an initial single injection of aflibercept and will be randomized if diabetic macular edema persists. Each subject will be evaluated for 6 months following randomization. Thus, the study duration will be 12 months plus the recruitment period. Subjects will be evaluated every month for safety, efficacy as measured by SDOCT and best corrected visual acuity (BCVA) using the Electronic Early Treatment Diabetic Retinopathy Study (E-ETDRS) protocol. In addition, ultra-widefield angiography will be performed at run-in visit, baseline, month 3, and month 6.
This description comes directly from the study's public registry record.
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No contact information is available for this study as per the public registry record.
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Locations (1)
| Retina Consultants of Houston | Houston, Texas, United States | — |
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Source record: clinicaltrials.gov/study/NCT04411693