The Effect of Bevacizumab on Corneal Neovascularization
- Sponsor
- Instituto de Olhos de Goiania
- Study ID
- NCT00797303
- Phase
- PHASE4
- Status
- Completed
Conditions
- Corneal Neovascularization
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 65 Years
- Healthy Volunteers
- Accepted
Interventions
- Bevacizumab — DRUGsubconjunctival injection of 1.25 mg bevacizumab and had a follow-up of at least 2 months
Study Details
Eight patients with corneal neovascularization were treated with subconjunctival injection of 1.25 mg bevacizumab and had a follow-up of at least 2 months. All patients had persistent corneal neovascularization for at least 6 months unresponsive to other treatments. Patients were monitored by ophthalmic exam and anterior segment photography.
Key Dates
- First listed
- Nov 25, 2008
- Start date
- Jan 31, 2006
- Status verified
- Nov 2011
- Primary completion
- Jul 31, 2008
- Completion
- Nov 30, 2008
Study Design
- Enrollment
- 8 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: 1A single intraoperative subconjunctival application of bevacizumab and 2 months follow-up
Primary Outcome Measure
The Effect of Bevacizumab on Corneal Neovascularization [ Time Frame: Compare the results ]
Related Studies
- Corneal Crosslinking for Treatment of Corneal NeovascularizationPHASE2/PHASE3 · Recruiting · Price Vision Group · Indianapolis, Indiana