Status:

COMPLETED

Bevacizumab Intravitreal for Myopic Choroidal Neovascularization

Lead Sponsor:

Instituto de Olhos de Goiania

Conditions:

Myopic Choroidal Neovascularization

Eligibility:

All Genders

21-65 years

Phase:

PHASE4

Brief Summary

To evaluate the clinical results of anti-VEGF intra-vitreal injections (IVT) in CNV secondary to pathologic myopia (PM-CNV).

Detailed Description

Nineteen consecutive patients (19 eyes) with subfoveal PM-CNV, 18 of whom had been unsuccessfully treated with Visudyne PDT, were treated with IVT of 1.25 mg bevacizumab or 0.5mg ranibizumab. ETDRS be...

Eligibility Criteria

Inclusion

  • Myopic CNVM,

Exclusion

  • Patients with poor compliance
  • Patients with uncontrolled diabetes and hypertension or any other medical condition that increase the risk of complications like recent history of Stroke or myocardial infraction (\< one year). (Physician clearance was obtained for all patients).
  • Age related macular degeneration with Juxtafoveal and Subfoveal CNVM: Recurrent CNVM following PDT and TTT with IVTA. Patient who could not afford PDT, Macugen or Lucentis which is FDA approved.
  • Patients who had undergone major surgery 28 days before, were excluded from the study and it was also suspended prior to elective surgery.
  • Refractory macular oedema due to vein occlusion, Pseudophakia, Clinically significant macular oedema (CSME) etc. that affects vision and does not respond adequately to usual treatment methods.
  • Proliferative diabetic retinopathy, non-resolving vitreous haemorrhage with PDR.
  • Idiopathic CNVM, Inflammatory CNVM and other conditions associated with CNVM.

Key Trial Info

Start Date :

January 1 2007

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

November 1 2008

Estimated Enrollment :

5 Patients enrolled

Trial Details

Trial ID

NCT00797992

Start Date

January 1 2007

End Date

November 1 2008

Last Update

November 25 2008

Active Locations (1)

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Instituto de Olhos de Goiania

Goiânia, Goiás, Brazil, 74120-050