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Intravitreal Bevacizumab in Recalcitrant Inflammatory Ocular Neovascularization

Intravitreal Bevacizumab in Recalcitrant Inflammatory Ocular Neovascularization: Multicenter Collaborative Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00645697
Acronym
AVA-ION
Enrollment
100
Registered
2008-03-28
Start date
2007-01-31
Completion date
2008-03-31
Last updated
2008-03-28

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

Conditions

Harada Toxoplasmosis, Multifocal Serpiginous Choroiditis, Neovascularization, Tuberculosis

Keywords

tuberculosis, Multifocal serpiginous choroiditis, histoplasmosis, Harada toxoplasmosis

Brief summary

One complication of uveitis which is driven by an increase in VEGF is the formation of inflammatory ocular neovascularization (ION). Here, we analyze the therapeutic role of intravitreal bevacizumab in ION not responding to standard therapy (systemic and ocular corticosteroids and systemic immunosuppressants) in a multicenter retrospective study.The natural history of subfoveal choroidal new vessels histoplasmosis, multifocal choroiditis, Harada and other inflammatory chorioretinal disorders has been very guarded, but with this new approach, we hope to stop the visual loss in these relatively young patients.

Detailed description

Members of the American Society of Retinal specialists, the American Uveitis Society and the International Uveitis Society were invited to contribute their consecutive cases of ION not responding to standard therapy (corticosteroids (CST) 4 or immunosuppression) and treated with intravitreal anti-VEGF agents. Cases with concomitant or prior cystoid macular edema, diabetes mellitus, or age-related macular degeneration were excluded. Most of the patients had initially been treated in a stepwise fashion with high doses of oral CST, with or without intraocular or subtenon CST or immunosuppressive therapy (as monitored by a rheumatologist). All patients opted to intravitreal anti-VEGF treatment after detailed information about the limited experience, potential side effects and the off-label character of the drug. The risks and benefits of intravitreal therapy were discussed with the patients (or their guardians) who signed an informed consent. Primary outcome measure: Best corrected visual acuity measured as logMAR. Secondary outcome measures:macular thickness on OCT, and stoppage of leakage by IVFA.

Interventions

None listed

Sponsors

Heidelberg University
CollaboratorOTHER
University Hospital Tuebingen
CollaboratorOTHER
University Hospital Freiburg
CollaboratorOTHER
Rafic Hariri University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Inflammatory ocular neovascularization (INO)

Exclusion criteria

* Eyes with age-related macular degeneration * Diabetes mellitus * Prior cystoid macular edema * Uncontrolled systemic hypertension * Cardiovascular disease

Design outcomes

Primary

MeasureTime frame
Best corrected visual acuity gain after bevacizumab therapy.3 month, 1 year, 2 year

Secondary

MeasureTime frame
fluorescein leakage of ocular neovascularization by fluorescein angiography and macular thickness by Optical Computed tomography.3 month

Countries

Lebanon

Outcome results

None listed

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