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
| Type | Name | Description |
|---|---|---|
| DRUG | Injection | Intravitreal 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.