A Phase 4 interventional study of Ranibizumab in Visual Impairment and Macular Edema, sponsored by Novartis Pharmaceuticals. Completed at 43 sites in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2017-02-23.
Sponsored by Novartis Pharmaceuticals · Phase 4, Interventional, and Treatment
The purpose of this study is to evaluate the proportion of patients with a 10 letters gain on Best Corrected Visual Acuity (BCVA) at 6 months in current medical practice.
308 studies on the registry are indexed under Vision Disorders; 81 are open to participants now.
This study's enrollment of 394 is above the median of 66 across 211 interventional studies indexed under Vision Disorders.
Browse Vision Disorders studies →Novartis Pharmaceuticals is the lead sponsor of 2,673 studies on the registry; 228 are open to participants now.
Of its 576 completed or terminated interventional studies of FDA-regulated products, 431 (75%) have results posted.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Ocular concomitant conditions/ diseases
Other protocol-defined inclusion/exclusion criteria may apply
Drug: Ranibizumab
proportion of patients with a 10 letters gain on Best Corrected Visual Acuity (BCVA)
Time frame: 6 months
mean average change in BCVA from baseline
Time frame: 6 months
if the letters gain after 2 injections is predictive from the letters gain at 6 months
Time frame: 6 months
mean number of injections needed to obtain a 10 letters gain
Time frame: 6 months
mean number of injections needed to obtain a stable visual acuity for three consecutive monthly assessments
Time frame: 6 months
efficacy of ranibizumab IVT on Central Retinal Thickness (OCT)
Time frame: 6 months
This study is completed, as verified in Feb 2017. You cannot join it, but the record below documents what was studied.
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Novartis Pharmaceuticals