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Intravitreal Bevacizumab for Neovascular Glaucoma

Intravitreal Bevacizumab for Neovascular Glaucoma; a Randomized Placebo Controlled Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00384631
Acronym
IVB NVG
Enrollment
26
Registered
2006-10-06
Start date
2006-04-30
Completion date
2007-03-31
Last updated
2008-02-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glaucoma, Neovascular

Keywords

Neovascular, Glaucoma, Bevacizumab, Avastin, Intravitreal, IOP

Brief summary

Several studies have confirmed high levels of vascular endothelial growth factor (VEGF) in eyes with neovascular glaucoma (NVG). The role of VEGF inhibitors in regression of other neovascular disorders such as wet-type age-related macular degeneration and diabetic macular edema has been described. We aim to evaluate the effect of three intravitreal injections of bevacizumab (Avastin) 2.5 mg versus a sham procedure for treatment of NVG. Outcome measures include intraocular pressure and extent of iris neovascularization. Both study arms will receive conventional treatment for NVG.

Interventions

OTHERsubconjunctival normal saline

0.1cc normal saline injection in the subconjunctival space repeated twice at monthly intervals

DRUGAvastin

intravitreal injection of avastin 2.5mg repeated twice at monthly intervals

Sponsors

Shahid Beheshti University of Medical Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
10 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Clinical diagnosis of NVG * Vision less than 20/200 * age 10-80 years

Exclusion criteria

* Uncontrolled Blood Pressure * History of thromboembolism * Congestive Heart Failure * Renal Failure * Pregnancy or Lactation * Active ocular or periocular infection * No light perception

Design outcomes

Primary

MeasureTime frame
Change in intraocular pressure6 months
Change in extent of iris neovascularization6 months

Secondary

MeasureTime frame
Best corrected visual acuity6 months

Countries

Iran

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026