Multifocal Electrophysiologic Findings After Intravitreal Bevacizumab(Avastin)Treatment
- Sponsor
- Asociación para Evitar la Ceguera en México
- Study ID
- NCT00417833
- Phase
- PHASE2/PHASE3
- Status
- Terminated
Conditions
- Choroidal Neovascularization
- Diabetic Proliferative Retinopathy
- Vascular Vein Oclussion
Eligibility Criteria
- Sex
- ALL
- Age
- N/A - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Intravitreal Bevacizumab — DRUG
Study Details
Purpose: Determine the short-term safety of intravitreal bevacizumab by multifocal electroretinography (mf-ERG). Methods: 120 eyes with choroidal neovascularization, proliferative diabetic retinopathy and retinal vein occlusion received intravitreal bevacizumab (2.5mg/0.1cc). All patients underwent best corrected visual acuity, fluorescein angiography, optical coherent tomography and mf-ERG before and 1 month after treatment.
Key Dates
- First listed
- Jan 4, 2007
- Start date
- Dec 31, 2005
- Status verified
- May 2024
- Completion
- Jul 31, 2006
Study Design
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
Related Studies
- A Clinical Trial of EYE201/MK-8748 in People With Macular Degeneration (MK-8748-002)PHASE2/PHASE3 · Recruiting · EyeBiotech Ltd. · Scottsdale, Arizona
- A Clinical Trial of EYE201/MK-8748 in People With Macular Degeneration (MK-8748-003)PHASE2/PHASE3 · Recruiting · EyeBiotech Ltd. · Gilbert, Arizona