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Bevacizumab and Photodynamic Therapy in Neovascular Age Related Macular Degeneration

Effects of Intravitreal Injection of Bevacizumab in Combination With Verteporfin Photodynamic Therapy

Status
Terminated
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00347399
Enrollment
25
Registered
2006-07-04
Start date
2006-03-31
Completion date
2007-06-30
Last updated
2024-05-30

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

Conditions

Age Related Macular Degeneration

Keywords

macular degeneration, antibodies, angiogenesis inhibitor

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

Interventions

Sponsors

Asociación para Evitar la Ceguera en México
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
55 Years to 99 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Visual acuity improvement at 6 monthsundefinedundefined

Secondary

MeasureTime frameDescription
Retinal thickness improvement at 6 monthsundefinedundefined

Countries

Mexico

Outcome results

None listed

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