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Clinical Trial Summary

This study is aimed to compare the effect of combined intravitreal Bevacizumab and Fasudil injection with Bevacizumab only injection in patients with persistant macular edema secondary to ratinal vein occlusion.

Methods:

In this study patients with retinal vein occlusion patient who had at least three or more intravitreal AntiVEGF injection with persistence of macular edema at funduscopic examination is recruited. The eligible patients in randomized in two groups "Bevacizumab" and "Bavacizumab + Fasudil" and in injected intravitreally for 3 times monthly. In "Bevacizumab+Fasudil" group patients receive two injections at each session Bavacizumab and Fasudil. In "Bevacizumab" group patients receive only Bevacizumab. The patients are followed for 6 months and central macular thickness and visual acuity is measured at baseline and monthly for 6 month. Baseline ancillary exams include Fluorescein Angiography and OCT-Angiography which is performed at the final exam as well. Patients needing any therapeutic intervention is addressed during the 6 month follow up period.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03391219
Study type Interventional
Source Shahid Beheshti University of Medical Sciences
Contact Ramin Noorinia, MD
Phone 982122591616
Email labbafi@hotmail.com
Status Recruiting
Phase Phase 2/Phase 3
Start date January 2018
Completion date October 2018

See also
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