drugset / Trial / NCT00811200

Treatment Of Radiation Retinopathy Trial

NCT00811200

RandomizedParallel-groupSingle-blindTreatment

Summary

The purpose of this study is to demonstrate a statistically significant improvement of visual acuity after treatment using either Lucentis® or Triamcinolone® compared to no treatment, in patients with radiation retinopathy.

Timeline

Start
2009-09
Primary completion
2012-01
Completion

Drugs

EvaluationDrugModalityDoseRoute
Comparator Ranibizumab Monoclonal antibody 0.5 mg Intravitreal
Comparator Triamcinolone Acetonide Other / unclassified 4 mg Intravitreal

Indications