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An open-label investigator research trial to study the safety and efficacy of a combination of a pro re nata regimen with fixed interval regimen intravitreal injections of ranibizumab in the treatment of choroidal neovascularization in subjects with neovascular age-related macular degeneration 31/12/2012

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The objective of this project is to explore the safety and efficacy of a combination of a pro re nata regimen with a fixed interval regimen of intravitreal ranibizumab injections in the treatment of choroidal neovascularization (CNV) in subjects with neovascular age related macular degeneration. Hypothesis: This reimen may have a benefit in the range of the monthly regimen but with a significantly smaller mean number of injections.    RESULTATS: The 12-month data presented support the hypothesis that the FUSION regimen for CNV secondary to exudative AMD provides visual benefit in the range of the monthly regimens but with a significantly smaller mean number of injections, even in patients in the current incident population presenting in clinical practices with higher levels of visual acuity, not reflected in previous trials, and therefore avoiding the visual limitations of the pro re nata regimens in AMD.

Inyecciones intravítreasDMAE seca o atróficaDMAE exudativa o húmedaRetinografíaAutofluorescenciaAngiografía fluoresceínicaAngiografía con verde de indocianinaTomografía de coherencia óptica

Autor

Dr. Jordi Monés, M.D., Ph.D.
Número de Colegiado COMB: 22.838
Director
Doctor en Medicina y Cirugía
Especialista en Oftalmología
Especialista en Retina, Mácula y Vítreo

Última modificación: 23 Septiembre, 2020 - 10:32