Diabetic Macular Edema Clinical Trial
Official title:
Diabetic Macular Edema: Relevance of Staging Progression on Therapeutic Outcome
NCT number | NCT05080803 |
Other study ID # | ESASO |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | June 1, 2021 |
Est. completion date | July 26, 2022 |
Verified date | September 2023 |
Source | European School of Advanced Studies in Ophthalmology |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Retrospective multi-center observational study on functional and morphological outcome of initial therapy for DME according to ESASO Morphologic Classification.
Status | Completed |
Enrollment | 608 |
Est. completion date | July 26, 2022 |
Est. primary completion date | December 23, 2021 |
Accepts healthy volunteers | |
Gender | All |
Age group | 50 Years and older |
Eligibility | Inclusion Criteria. Eligible eyes at the retrospective review 1. Any stage of DME treated with a loading dose of 3 anti-VEGF (any type) or 1 IV dexamethasone (STEP 1). 2. OCT scans and retinal maps (radial/raster lines) at baseline (max 1 month before injection) and at one month (max 6 weeks) after the third anti-VEGF or at 3 months (max 16 weeks) after IV steroid injection (STEP 2). 3. VA at the time of both OCT examinations. Exclusion Criteria: 1. Past ocular surgery of any kind (except for cataract surgery) or ocular pathologies other than diabetic retinopathy. 2. Macular edema considered to be due to a cause other than diabetic macular edema. 3. OCT examination suggesting that vitreoretinal interface abnormalities (e.g., a taut posterior hyaloid or epiretinal membrane) are the primary cause of the macular edema. In the case of ERM, an OCT scan must be sent to the Coordinating Center for approval. 4. Any ocular pathology or ocular condition other than diabetes that in the opinion of the investigator might affect macular edema. 5. History of any therapy (anti-VEGF treatment, focal/grid macular photocoagulation, intravitreous or peribulbar corticosteroids) for DME or diabetic retinopathy in the past 8 months. 6. History of YAG capsulotomy performed within two months before enrollment. |
Country | Name | City | State |
---|---|---|---|
Switzerland | ESASO Scientific Projects | Lugano |
Lead Sponsor | Collaborator |
---|---|
European School of Advanced Studies in Ophthalmology |
Switzerland,
Panozzo G, Cicinelli MV, Augustin AJ, Battaglia Parodi M, Cunha-Vaz J, Guarnaccia G, Kodjikian L, Jampol LM, Junemann A, Lanzetta P, Lowenstein A, Midena E, Navarro R, Querques G, Ricci F, Schmidt-Erfurth U, Silva RMD, Sivaprasad S, Varano M, Virgili G, Bandello F. An optical coherence tomography-based grading of diabetic maculopathy proposed by an international expert panel: The European School for Advanced Studies in Ophthalmology classification. Eur J Ophthalmol. 2020 Jan;30(1):8-18. doi: 10.1177/1120672119880394. Epub 2019 Nov 12. — View Citation
Panozzo G, Mura GD, Franzolin E, Giannarelli D, Albano V, Alessio G, Arrigo A, Casati S, Cassottana P, Contardi C, D'Aloisio R, Fasce F, Gusson E, Marchini G, Mastropasqua L, Niccolo M, Palmisano C, Pastore MR, Saviano S, Tognetto D, Bandello F. Early DMO: a predictor of poor outcomes following cataract surgery in diabetic patients. The DICAT-II study. Eye (Lond). 2022 Aug;36(8):1687-1693. doi: 10.1038/s41433-021-01718-4. Epub 2021 Aug 3. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Functional and morphological improvement in DME after initial therapeutic loading phase, according to ESASO stage of progression of the disease. | Visual acuity and morphological (OCT) stage of the disease (as described in ESASO DME classification) will be evaluated at time 0 and four months after the first injection of intravitreal dexamethasone or one month after the loading phase (3 monthly injections) with anti-VEGF. | Four months | |
Secondary | Validation of ESASO DME staging classification | After preliminary instruction on ESASO Staging system of DME, participating centers will evaluate the stage of DME at time 0 of every eye retrospectically selected to participate to the study. This staging will be than validated by the Coordinating Center, and the total concordance of staging (K index) will be used to validate the Classification | 3 months |
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