drugset / Trial / NCT00211393

A Pilot Study of the Treatment of Central Serous Chorioretinopathy With Ketoconazole

NCT00211393

Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the effect of an adrenocorticoid antagonist (ketoconazole), 600 mg per day for 4 weeks, in the treatment of patients with central serous chorioretinopathy (CSC).

Timeline

Start
2005-05
Primary completion
2008-03
Completion
2008-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Ketoconazole Small molecule 600 mg Oral