Lucentis for New Onset Neovascular Glaucoma
- Sponsor
- University of Illinois at Chicago
- Study ID
- NCT00727038
- Phase
- PHASE1/PHASE2
- Status
- Withdrawn
Conditions
- Glaucoma
- Neovascular Glaucoma
- New Onset Glaucoma
- New Onset Neovascular Glaucoma
Eligibility Criteria
- Sex
- ALL
- Age
- 21 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Ranibizumab (Lucentis) — DRUG0.5 mg ranibizumab intravitreal injection single dose administration
Study Details
Neovascular glaucoma is a potentially debilitating disease of the eye. Vascular eye disease such as diabetes and vein occlusions can cause the retina to release factors that promote the growth of abnormal blood vessels. These abnormal vessels can grow in the drainage mechanism of the eye causing pressure in the eye to markedly increase. This can potentially cause irreversible damage to the optic nerve from glaucoma leading to permanent blindness and painful eyes. Conventional treatments including laser and freezing therapy take weeks to cause regression in abnormal blood vessel growth. This delay often results in permanent vision loss and pain. New medications targeted at more immediately reducing blood vessel growth may aid in the treatment of this disease.
Key Dates
- First listed
- Aug 1, 2008
- Start date
- Jan 4, 2008
- Status verified
- Jul 2008
- Primary completion
- May 15, 2009
- Completion
- May 15, 2009
Study Design
- Enrollment
- 0 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: 1Lucentis (ranibizumab) with conventional treatment
- No Intervention: 2Conventional treatment
Primary Outcome Measure
Mean change in best corrected visual acuity (BCVA) as assessed by the number of letters read correctly on the ETDRS eye chart at a starting test distance of 4 meters from baseline to Month 6. [ Time Frame: Baseline to Month 6. ]
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