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Intravitreal Bevacizumab for Diabetic Retinopathy

Efficacy of Intravitreal Bevacizumab for Severe Nonproliferative and Proliferative Diabetic Retinopathy.

Status
Terminated
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00600262
Enrollment
Unknown
Registered
2008-01-24
Start date
2005-12-31
Completion date
2006-06-30
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

Active Photocoagulated Diabetic Retinopathy, Proliferative Diabetic Retinopathy, Severe Nonproliferative

Keywords

severe nonproliferative, proliferative diabetic retinopathy, active photocoagulated diabetic retinopathy, intravitreal bevacizumab

Brief summary

Background: to evaluate the 3-month efficacy of a single dose of intravitreal bevacizumab on the progression of severe non proliferative diabetic retinopathy, proliferative diabetic retinopathy and active photocoagulated diabetic proliferative by evaluation of ischemic areas and regression of retinal and disc neovasculrization. Methods: 40 patients were enrolled in a prospective, interventional study. Patients were treated with intravitreal bevacizumab 0.1ml (0.25mg). We evaluated visual acuity, neovascularization leakage points, capillary closure ischemic areas and macular edema by clinical examination and fluorescein angiography. A clinical examination was performed at baseline and days 1,14 and 30. Active leakage points were measured by fluorescein angiography at 30 days.

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
Healthy volunteers
No

Inclusion criteria

* Severe nonproliferative * Proliferative diabetic retinopathy * Active photocoagulated diabetic retinopathy

Exclusion criteria

* Previous vascular occlusion * Glaucoma * Uncontrolled hypertension, thromboembolic event * Renal abnormalities * Recent or planned surgery * Coagulation abnormalities * Panretinal photocoagulation of less than one month before * Patients with known serious allergies

Countries

Mexico

Outcome results

None listed

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