Clinical Trials Directory

Trials / Completed

CompletedNCT02641457

Intravitreal Aflibercept or Ranibizumab for Rubeosis Iridis

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
2 (actual)
Sponsor
Instituto de Olhos de Goiania · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

Aflibercept (Eylea®) and ranibizumab (Lucentis®) are an anti-VEGF, but there are differences between the two drugs. To determine and compare whether intraocular aflibercept and ranibizumab decreases rubeosis iridis (RI) in patients with neovascular glaucoma (NVG).

Detailed description

Aflibercept (Eylea®) and ranibizumab (Lucentis®) are an anti-VEGF, but there are differences between the two drugs. Lucentis is administered in the form of smaller molecules, which is thought to give Lucentis an advantage over Eylea in its ability to penetrate the eye's retina and halt abnormal blood vessel growth contributing to advanced macular degeneration and scarring that causes blindness. They may have a role in treating ocular disorders involving fibrovascular proliferation. To determine and compare whether intraocular aflibercept and ranibizumab decreases rubeosis iridis (RI) in patients with neovascular glaucoma (NVG).

Conditions

Interventions

TypeNameDescription
DRUGAflibercept12 eyes received an intraocular injection of 2.00 mg of aflibercept (IA) and IOP were measured by tonometer. The neovascularization was evaluated by biomicroscope.
DRUGRanibizumab12 eyes received an intraocular injection of 1.25mg ranibizumab and IOP were measured by tonometer. The neovascularization was evaluated by biomicroscope.

Timeline

Start date
2014-03-01
Primary completion
2015-03-01
Completion
2015-10-01
First posted
2015-12-29
Last updated
2015-12-29

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT02641457. Inclusion in this directory is not an endorsement.