Intravitreal Bevacizumab for Polypoidal Choroidal Vasculopathy

• Status: Unknown status
• Trial end date: 2008-05-01
• Target enrollment: 0
• Participant gender: All

Summary

1. Primary objectives

a. To evaluate the Effects of intravitreal Bevacizumab on polypoidal choroidal vasculopathy(PCV)

2. Secondary objectives

1. To assess the changes in visual acuity

2. To assess the change in lesion characteristics of PCV

• size of PCV

• fluorescein leakage

• foveal thickness

3. To investigate the safety of intravitreal Bevacizumab in patients with PCV

4. To assess the effect of intravitreal Bevacizumab on the recurrence rate and the the incidence of submacular hemorrhage in patients with PCV

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Asan Medical Center
• Treatments: Bevacizumab

Criteria

Inclusion Criteria:

• Male or female, CNV secondary to PCV

• BCVA of 20/40 to 20/320 (Snellen equivalent)

• Evidence of presumed recent disease progression (blood, growth by FA, or recent VA loss)

Exclusion Criteria:

• Uncontrolled glaucoma or any other ocular condition that would prevent an improvement in visual acuity

• Media opacity in the study eye that precludes clinical and photographic evaluation

• Intraocular surgery < 1 month before day 0

• Use of heparin/warfarin within 1 month prior to injection

• Known allergy or hypersensitivity to fluorescein, indocyanine green or povidone iodine

• Contraindication to pupil dilation in either eye

• Any condition which precludes patients' ability to comply with study requirements including completion of the study