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UnknownNCT01246089

Ranibizumab for Myopic Neovascularization

Ranibizumabe Intravitreal Injection for Myopic Choroidal Neovascularization

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Instituto de Olhos de Goiania · Academic / Other
Sex
All
Age
21 Years – 65 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to evaluate the clinical results of anti-VEGF intra-vitreal injections (IVT) in CNV secondary to pathologic myopia (PM-CNV).

Detailed description

Twenty consecutive patients (30 eyes) with subfoveal PM-CNV, 9 of whom had been unsuccessfully treated with Visudyne PDT, were treated with IVT of 0.5mg ranibizumab. ETDRS best corrected visual acuity, macular thickness on OCT scans, and angiographic features were recorded and evaluated. The aspect of OCT scans passing across the PM-CNV was also analyzed. IVTs were repeated only in case of persistent angiographic leakage and if OCT scans showed retinal thickening or edema and serous retinal detachment. The follow-up period was at least 6 months.

Conditions

Interventions

TypeNameDescription
DRUGranibizumab injectionRanibizumab intravitreal injection of 0,5 mg ( 0.05mL)

Timeline

Start date
2009-07-01
Primary completion
2014-10-01
Completion
2014-11-01
First posted
2010-11-23
Last updated
2014-01-01

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT01246089. Inclusion in this directory is not an endorsement.

Ranibizumab for Myopic Neovascularization (NCT01246089) · Clinical Trials Directory