CompletedNot applicableNCT01990677
Eplerenone for the Treatment of Central Serous Chorioretinopathy
Studying Central serous chorioretinopathy
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Wills Eye
- Principal Investigator
- Mitchell Fineman, MDMid Atlantic Retina
- Intervention
- 25mg Eplerenone(drug)
- Enrollment
- 108 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2013 – 2015
Study locations (10)
- Mid Atlantic Retina, Cherry Hill, New Jersey, United States
- Mid Atlantic Retina, Marlton, New Jersey, United States
- Mid Atlantic Retina, Mays Landing, New Jersey, United States
- Mid Atlantic Retina, Bala-Cynwyd, Pennsylvania, United States
- Mid Atlantic Retina, Bethlehem, Pennsylvania, United States
- Mid Atlantic Retina, Huntingdon Valley, Pennsylvania, United States
- Mid Atlantic Retina, Lansdale, Pennsylvania, United States
- Mid Atlantic Retina, New Wilmington, Pennsylvania, United States
- Mid Atlantic Retina, Newtown Square, Pennsylvania, United States
- Mid Atlantic Retina, Plymouth Meeting, Pennsylvania, United States
Collaborators
Mid Atlantic Retina
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT01990677 on ClinicalTrials.govOther trials for Central serous chorioretinopathy
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