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Clinical Trial Summary

Purpose: The aim of this study is to evaluate the functional and anatomical effects of switching from Bevacizumab to Aflibercept in patients with persistent DME resistant to Bevacizumab.

Methods: Patients with DME refractory to Bevacizumab (1.25 mg/ 0.05 mL) were subsequently switched to Aflibercept (2.0 mg/0.05 ml). The included patients received 5 loading doses of intravitreal Aflibercept (2.0 mg/0.05 mL) (Eylea; Bayer, Berlin, Germany) given monthly. After the loading dose, Aflibercept was injected every 2 months. The follow up duration was one year.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03974425
Study type Interventional
Source University of Alexandria
Contact
Status Completed
Phase N/A
Start date April 1, 2016
Completion date April 1, 2018

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