Clinical Trials Directory

Trials / Completed

CompletedNCT00797992

Bevacizumab Intravitreal for Myopic Choroidal Neovascularization

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

Summary

To evaluate the clinical results of anti-VEGF intra-vitreal injections (IVT) in CNV secondary to pathologic myopia (PM-CNV).

Detailed description

Nineteen consecutive patients (19 eyes) with subfoveal PM-CNV, 18 of whom had been unsuccessfully treated with Visudyne PDT, were treated with IVT of 1.25 mg bevacizumab or 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
DRUGInjectionIntravitreal injection of 1.25 mg bevacizumab

Timeline

Start date
2007-01-01
Primary completion
2008-11-01
Completion
2008-11-01
First posted
2008-11-25
Last updated
2008-11-25

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT00797992. Inclusion in this directory is not an endorsement.

Bevacizumab Intravitreal for Myopic Choroidal Neovascularization (NCT00797992) · Clinical Trials Directory