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Safety and Effectiveness of Subconjunctival Injection of Bevacizumab in the Treatment of Corneal Neovasculization

The Application of Subconjunctival Injection of Bevacizumab (Avastin) in the Treatment of Corneal Neovasculization

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00681603
Enrollment
13
Registered
2008-05-21
Start date
2007-08-31
Completion date
2008-02-29
Last updated
2008-05-21

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

Conditions

Herpetic Keratopathy, Lipid Keratopathy, Penetrating Keratoplasty, Rosacea

Keywords

corneal neovascularization, lipid keratopathy, penetrating keratopathy, bevacizumab, Avastin, subconjunctival injection

Brief summary

1. Purpose:Our animal study demonstrated the effectiveness of subconjunctival injection of bevacizumab in the inhibition of corneal neovasculization formation. The purpose of this human interventional study is to report the treatment outcome of subconjunctival injection of bevacizumab in patients with corneal neovascularization. 2. Material and methods: We enrolled 13 patients with unilateral or bilateral clinically significant corneal neovascularization during Aug. 2007 to Jan. 2008. Subconjunctival injection of bevacizumab once per month for at most 7 times was performed according to clinical response. 3. Main outcome measurements: resolution of corneal neovascularization, reduction of lipid infiltrate, improved visual acuity.

Interventions

DRUGsubconjunctival injection of bevacizumab ( 1.25 to 2.50 mg)

subconjunctival injection of bevacizumab ( 1.25 to 2.50mg) according to the clinical judgment. Once per months for three times then reevaluate the drug effect, if the response was adequate, stop the trial; if no improvement, another three month intervention would be performed.

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Age
10 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Significant unilateral or bilateral corneal neovascularization that extending over the limbus at least 2mm * The underlying etiologies that caused corneal neovascularization included post penetrating keratoplasty (PKP), trauma, infectious or non-infectious corneal ulcer, post-keratoplasty, etc. * Corneal neovascularization induced lipid keratopathy, corneal edema, or irregular corneal surface. The best-corrected visual acuity was less than 20/25 * Post-PKP corneal neovascularization that had no associated lipid keratopathy, no corneal edema, or corneal irregularity. But the neovascularization was highly possible to cause graft rejection. * The corneal neovascularization was refractory to other medical treatment * The patient had received PKP or other corneal surgeries more than half a year ago and was not in the acute post-operation phase * The patient had no active endopthalmitis, glaucoma with uncontrolled intraocular pressure, or vitreoretinal diseases * The patient signed inform consent to have regular follow up and treatment

Exclusion criteria

* The neovascularization had clinical improvement three months before the first injection * The lipid keratopathy had clinical improvement three months before the first injection * The patient that suspected to have poor visual outcome or had already been light sense negative * Glaucoma patient that had uncontrolled intraocular pressure * Poor corneal epithelialization * Post-PKP patient that had graft failure or rejection * Patient that had systemic disease which was not suitable for bevacizumab use * Pregnant patient

Design outcomes

Primary

MeasureTime frame
Resolution of corneal neovascularization, reduction of lipid infiltrate, improved visual acuityprospective

Secondary

MeasureTime frame
major side effectsprospective

Countries

Taiwan

Outcome results

None listed

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