Effectiveness and Safety of Topical Ranibizumab for Treatment of Corneal Neovascularization (NV)
Part of paid clinical trials in Boston, Massachusetts.
- Sponsor
- Reza Dana, MD
- Study ID
- NCT00681889
- Phase
- PHASE1
- Status
- Completed
Conditions
- Corneal Neovascularization
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Ranibizumab — DRUG10 Patients will receive treatment (Ranibizumab)
Study Details
The purpose of this study is to determine the effectiveness and safety of ranibizumab (Lucentis) in treatment of corneal neovascularization.
Key Dates
- First listed
- May 21, 2008
- Start date
- Apr 30, 2008
- Status verified
- Oct 2012
- Primary completion
- Sep 30, 2009
- Completion
- Sep 30, 2010
Study Design
- Enrollment
- 9 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Treatment Arm10 Patients will receive treatment (Ranibizumab)
Primary Outcome Measure
Incidence and Severity of Ocular Adverse Event [ Time Frame: 16 Weeks ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Massachusetts Eye and Ear Infirmary | Boston | Massachusetts | 02114 | - |
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