Eplerenone for the Treatment of Central Serous Chorioretinopathy

NACompletedINTERVENTIONAL
Enrollment

108

Participants

Timeline

Start Date

October 31, 2013

Primary Completion Date

March 31, 2015

Study Completion Date

May 31, 2015

Conditions
Central Serous Chorioretinopathy
Interventions
DRUG

25mg Eplerenone

Patients will be given 25mg Eplerenone (or 50mg Eplerenone) or placebo throughout the study and the dosage will be based on the serum potassium/creatine levels. Patients will be randomized 2:1 such that 36 patients in each group will receive eplerenone and 16 patients in each group will receive placebo

DRUG

Placebo

Patients will be given placebo throughout the study from day one, other patients may be tapered down to placebo based on the serum potassium/creatine levels. 16 patients in each group will receive placebo.

Trial Locations (10)

18020

Mid Atlantic Retina, Bethlehem

19004

Mid Atlantic Retina, Bala-Cynwyd

19006

Mid Atlantic Retina, Huntingdon Valley

19073

Mid Atlantic Retina, Newtown Square

19446

Mid Atlantic Retina, Lansdale

19462

Mid Atlantic Retina, Plymouth Meeting

19803

Mid Atlantic Retina, New Wilmington

08002

Mid Atlantic Retina, Cherry Hill

08053

Mid Atlantic Retina, Marlton

08330

Mid Atlantic Retina, Mays Landing

All Listed Sponsors
collaborator

Mid Atlantic Retina

OTHER

lead

Wills Eye

OTHER

NCT01990677 - Eplerenone for the Treatment of Central Serous Chorioretinopathy | Biotech Hunter | Biotech Hunter