drugset / Trial / NCT00802906

Bevacizumab Versus Micropulse in Central Serous Chorioretinopathy (CSC)

NCT00802906

Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the clinical efficacy of an initial subthreshold retinal micropulselasercoagulation versus a single intravitreal 1.5mg bevacizumab injection in central serous choriretinopathy, as the micropulse will selectively treat the damaged RPE to induce reproliferation of healthy RPE cells, whereas the intravitreal injection should non-selectively stop the RPE leakage.

Timeline

Start
2007-05
Primary completion
2010-11
Completion
2010-12

Drugs

EvaluationDrugModalityDoseRoute
Comparator Bevacizumab Monoclonal antibody 1.5 mg Intravitreal