The aim of the study is to determine the efficacy and safety in treating patients with chronic central serous chorioretinopathy with the drug eplerenone.
* The goal of the study is to examine the short-term effects and safety of eplerenone, a systemic anti-aldosterone medication, in a group of patients with central serous chorioretinopathy (CSCR). * There is currently no standard treatment or therapy for chronic CSCR, a potentially debilitating eye disease. * There is evidence that high blood serum corticosteroid levels can cause or worsen CSCR * Eplerenone, a mineralocorticoid receptor antagonist, has been shown to be of visual and anatomic benefit in a small series of 4 patients with chronic CSCR, suggesting that decreasing mineralocorticoid action in the eye may improve signs and symptoms of CSCR * The study's aim is to evaluate a standardized dose of eplerenone in a controlled prospective fashion for chronic CSCR. * The study consists of taking a standard dose of eplerenone, 25mg once daily for a week, followed by 50mg once daily, for a total of 3 months * Patients will be monitored for efficacy and side effects from the beginning of treatment and for 6 months
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
30
Tel Aviv Souraski Medical Center
Tel Aviv, Israel, Israel
RECRUITINGDecrease of at least 10% in subretinal fluid thickness as measured by optical coherence tomography (OCT)
Time frame: 6 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.