Overview

Lucentis for New Onset Neovascular Glaucoma

Status:
Withdrawn
Trial end date:
2009-05-15
Target enrollment:
0
Participant gender:
All
Summary
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.
Phase:
Phase 1/Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University of Illinois at Chicago
Collaborator:
Genentech, Inc.
Treatments:
Ranibizumab
Criteria
Inclusion Criteria:

- Ability to provide written informed consent and comply with study assessments for the
full duration of the study

- Age > 21 years

- Diagnosis of neovascular glaucoma (angle neovascularization with or without iris
neovascularization and IOP > 21 mm Hg and > 5 mm Hg IOP compared to the fellow eye).

- Neovascular glaucoma secondary to retinal ischemia (central retinal vein occlusion,
proliferative diabetic retinopathy, ocular ischemic syndrome, etc.)

Exclusion Criteria:

- Pregnancy (positive pregnancy test) or lactation or pre-menopausal women not using
adequate contraception. The following are considered effective means of contraception:
surgical sterilization or use of oral contraceptives, barrier contraception with
either a condom or diaphragm in conjunction with spermicidal gel, an IUD, or
contraceptive hormone implant or patch.

- Prior enrollment in the study

- Any other condition that the investigator believes would pose a significant hazard to
the subject if the investigational therapy were initiated

- Participation in another simultaneous medical investigation or trial

- > 270 degrees of closed trabecular meshwork (closure secondary to peripheral anterior
synechiae)

- History of active inflammatory, infectious, or idiopathic keratitis precluding view of
the anterior segment structures.

- Previous intravitreal injections of ranibizumab or bevacizumab in either eye.