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Eplerenone for the Treatment of Central Serous Chorioretinopathy
NCT01990677 · View on ClinicalTrials.gov ↗
Study Summary
To test the effect oral eplerenone versus placebo in patients with central serious chorioretinopathy .
Conditions Studied
Interventions
- DRUG Placebo
- DRUG 25mg Eplerenone
Study Locations (10)
Pennsylvania
- Mid Atlantic Retina — Bala-Cynwyd
- Mid Atlantic Retina — Bethlehem
- Mid Atlantic Retina — Huntingdon Valley
- Mid Atlantic Retina — Lansdale
- Mid Atlantic Retina — New Wilmington
- Mid Atlantic Retina — Newtown Square
- Mid Atlantic Retina — Plymouth Meeting
New Jersey
- Mid Atlantic Retina — Cherry Hill
- Mid Atlantic Retina — Marlton
- Mid Atlantic Retina — Mays Landing
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 108 participants |
| Start Date | 2013-10 |
| Est. Completion | 2015-05 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01990677
The ClinicalTrials.gov registry entry for NCT01990677 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 108 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wills Eye, which has 12 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Central Serous Chorioretinopathy appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT01990677 reports 10 study locations spanning 2 distinct geographic areas — top geographies include Pennsylvania, New Jersey. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT01990677 about?
NCT01990677 is a clinical study titled "Eplerenone for the Treatment of Central Serous Chorioretinopathy". To test the effect oral eplerenone versus placebo in patients with central serious chorioretinopathy .
What is the current status of trial NCT01990677?
This trial is currently completed. It is a NA study. The enrollment target is 108 participants. The study started on 2013-10. Estimated completion is 2015-05.
What conditions does trial NCT01990677 study?
This clinical trial studies the following conditions: Central Serous Chorioretinopathy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT01990677?
The interventions under investigation include: Placebo (DRUG), 25mg Eplerenone (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT01990677?
This trial is sponsored by Wills Eye, which has 12 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT01990677 being conducted?
This trial has 10 study locations across New Jersey, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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