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Bevacizumab and Photodynamic Therapy in Neovascular Age Related Macular Degeneration

Phase 2
Terminated
Conditions
Age Related Macular Degeneration
Registration Number
NCT00347399
Lead Sponsor
Asociación para Evitar la Ceguera en México
Brief Summary

The purpose of this study is to determine if of combination therapy of intravitreal bevacizumab 4 days after the application of photodynamic therapy could improve the visual outcomes of patients with neovascular age related macular degeneration.

Detailed Description

The neovascular age related macular degeneration(AMD) is a important cause of legal blindness in adults older than 50 years. Currently the treatment is photodynamic therapy that offer stabilization and limited visual improvement after 2 years of therapy. Bevacizumab has been reported effective used as intravenous injection for AMD. But serious side effects have been reported with the use of this drug in oncologic patients. The intravitreal use has been reported in limited case reports and safety and efficacy should be determined. The purpose of this study is efficacy and safety of 2.5 mg intravitreal of bevacizumab for AMD 4 days after photodynamic therapy with verteporfin

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
25
Inclusion Criteria

55 years old neovascular Age related acular degeneration subfoveolar neovascular membrane best corrected visual acuity better than 20/200 snellen (1.0 logMAR)

Exclusion Criteria
  • Previously treated eyes glaucoma diabetes mellitus uncontrolled hypertension coronary artery disease

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Visual acuity improvement at 6 monthsundefined

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Secondary Outcome Measures
NameTimeMethod
Retinal thickness improvement at 6 monthsundefined

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Trial Locations

Locations (1)

Hospital Luis Sanchez Bulnes

🇲🇽

Mexico city, DF, Mexico

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