Intravitreal Bevacizumab for Diabetic Retinopathy

Last updated: May 29, 2024
Sponsor: Asociación para Evitar la Ceguera en México
Overall Status: Terminated

Phase

2/3

Condition

Diabetic Retinopathy

Retina

Diabetic Vitreous Hemorrhage

Treatment

intravitreal bevacizumab

Clinical Study ID

NCT00600262
APEC-004
  • All Genders

Study 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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Severe nonproliferative

  • Proliferative diabetic retinopathy

  • Active photocoagulated diabetic retinopathy

Exclusion

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

Study Design

Treatment Group(s): 1
Primary Treatment: intravitreal bevacizumab
Phase: 2/3
Study Start date:
December 01, 2005
Estimated Completion Date:
June 30, 2006

Connect with a study center

  • Elizabeth Reyna Castelan

    Mexico City, 04030
    Mexico

    Site Not Available

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