drugset / Trial / NCT00802906
Bevacizumab Versus Micropulse in Central Serous Chorioretinopathy (CSC)
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Bevacizumab | Monoclonal antibody | 1.5 mg | Intravitreal |