Treatment of Failing Blebs With Ranibizumab



Status:Recruiting
Conditions:Ocular
Therapuetic Areas:Ophthalmology
Healthy:No
Age Range:40 - Any
Updated:11/8/2014
Start Date:June 2007
Contact:Jeffrey Liebmann, MD
Email:JML18@earthlink.net
Phone:212-477-7540

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Effect of Needle Bleb Revision With Ranibizumab as a Primary Intervention in a Failing Bleb Following Trabeculectomy

This study was designed to evaluate the efficacy and safety in the use of Ranibizumab, an
effective vascular endothelial growth factor (VGEF) inhibitor, in treating patients with a
failing bleb, characterized by increased fibrosis and vascularization of the conjuctiva,
following trabeculectomy. Six subjects from one site will be enrolled in this study.


Inclusion Criteria:

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

- Age > 40 years

- Patients with Open-angle Glaucoma who have had trabeculectomy

- Patients determined to have failing bleb with presence of superficial bleb
vascularity and IOP increase on 3 successive visits without topical medication

- Patients whose intraocular pressure (IOP) is above goal IOP after suture lysis and
digital compression have been attempted

Exclusion Criteria:

- Pregnancy (positive pregnancy test) or lactation.

- Premenopausal 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.

- Current infection or inflammation in either eye

- Any abnormality preventing reliable applanation tonometry in either eye

- Other non-glaucomatous disease affecting visual field, (pituitary lesions,
demyelinating disease, congenital optic nerve anomaly, prior retinal and optic nerve
vascular occlusive disease, retinal dystrophy and degeneration, diabetes and HIV and
AIDS infection)

- Strabismus, nystagmus, monocular patient

- 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
We found this trial at
1
site
New York, New York 10003
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from
New York, NY
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