drugset / Trial / NCT02354170

Short-Term Oral Mifepristone for Central Serous Chorioretinopathy

NCT02354170

RandomizedSingle-groupDouble-blindTreatment

Summary

The goal of the study is to assess the efficacy and safety of mifepristone 300 or 900-mg once-daily dosing by mouth for 4 weeks in patients with central serous chorioretinopathy.

Timeline

Start
2015-01
Primary completion
2017-04-27
Completion
2017-04-27

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Mifepristone Small molecule 300 mg Oral
Subject Mifepristone Small molecule 900 mg Oral