Aflibercept Intravitreal Injection for Myopic Choroidal Neovascularization
- Sponsor
- Instituto de Olhos de Goiania
- Study ID
- NCT02033018
- Phase
- PHASE4
- Status
- Unknown
Conditions
- Choroidal Retinal Neovascularization
Eligibility Criteria
- Sex
- ALL
- Age
- 21 Years - 65 Years
- Healthy Volunteers
- Accepted
Interventions
- Aflibercept Injection — DRUGAflibercept intravitreal injection
Study Details
The purpose of this study is to evaluate the clinical results of anti-VEGF intra-vitreal injections (IVT) in CNV secondary
Key Dates
- Start date
- Oct 31, 2013
- Status verified
- Jan 2014
- Primary completion
- Nov 30, 2014
- Completion
- Nov 30, 2014
Study Design
- Enrollment
- 20 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Aflibercept injectionMyopic eyes with retinal neovascularization submitted a aflibercept intravitreal injection
Primary Outcome Measure
Efficacy [ Time Frame: To evaluate the clinical results of aflibercept intravitreal injection (AII) in choroidal neovascularization (CNV) secondary to pathologic myopia (PM-CNV), after 1 year follow up. ]
Central Contacts
- Raquel Monteiro55 62 3220 2500
- João J Nassaralla, Jr55 62 3220 2545