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NCT00417833 Clinical Trial

Multifocal Electrophysiologic Findings After Intravitreal Bevacizumab(Avastin)Treatment

Choroidal Neovascularization Clinical Trial

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT00417833
Other study ID # APEC-0017
Secondary ID
Status Terminated
Phase Phase 2/Phase 3
First received
Last updated
Start date December 2005
Est. completion date July 2006

Study information
Verified date May 2024
Source Asociación para Evitar la Ceguera en México
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Terminated
Enrollment 0
Est. completion date July 2006
Est. primary completion date
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Proliferative diabetic retinopathy, vascular vein oclussion, choroidal neovascularization - Multifocal electroretinogram before intravitreal bevacizumab and at 1,3, and 6 months after treatment - Completely studies Exclusion Criteria: Complications - Tractional Detachment - Endophthalmitis

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Intravitreal Bevacizumab

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Asociación para Evitar la Ceguera en México
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