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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.

Injections intravitréennesDMLA « sèche » ou atrophiqueDMLA exsudative ou humideRétinographieAutofluorescenceAngiographie en fluorescenceAngiographie au vert d’indocyanineTomographie par cohérence optique

Author

Dr Jordi Monés, médecin, titulaire d’un doctorat
Inscrit à l'ordre des médecins de Barcelone, sous le numéro 22838
Directeur
Docteur en médecine et chirurgie
Spécialiste en ophtalmologie
Spécialiste de la rétine, de la macula et du vitré

Last modified: 17 July, 2019 - 14:57