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Trial · NCT01990677

Eplerenone for the Treatment of Central Serous Chorioretinopathy

NCT01990677, Not applicable, Completed, Wills Eye; results first posted 2017-06-29

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Eplerenone for the Treatment of Central Serous Chorioretinopathy. Trials, record NCT01990677. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01990677

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Eplerenone for the Treatment of Central Serous Chorioretinopathy
NCT number
NCT01990677
Status
Completed
Phases
Not applicable
Enrollment
108 participants, actual
Lead sponsor
Wills Eye
Conditions
Central Serous Chorioretinopathy
Interventions
25mg Eplerenone, Placebo
First posted
2013-11-21
Last updated
2018-11-07
Results first posted
2017-06-29

Source ClinicalTrials.gov

Registered outcomes3

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryMean Change in Maximal Subretinal Fluid Height Based on Spectral Domain Optical Coherence Tomography (OCT) Measurement.Baseline and 2 monthsMean change in maximal subretinal fluid height based on spectral domain OCT from baseline to month 2 in chronic central serous chorioretinopathy (CSCR) patients receiving placebo versus eplerenone.
SecondaryMean Change in Subfoveal Fluid Height Based on OCT MeasurementBaseline and Month 2Mean change in subfoveal fluid height based on spectral domain OCT measurement from baseline to month 2 in chronic CSCR patients receiving placebo versus eplerenone.
OtherProportion of Eyes Demonstrating a Reduction in Subretinal Fluid on OCTBaseline and Month 2Proportion of eyes having a decrease in subretinal fluid on spectral domain OCT from baseline to month 2 in chronic CSCR patients receiving placebo versus eplerenone.

Outcomes3

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYMean Change in Maximal Subretinal Fluid Height Based on Spectral Domain Optical Coherence Tomography (OCT) Measurement.Baseline and 2 monthsSignificant acute data collection missing therefore only chronic arm data analysis was reviewed and entered into results data.micronsMEAN
SECONDARYMean Change in Subfoveal Fluid Height Based on OCT MeasurementBaseline and Month 2Significant acute data collection missing therefore only chronic arm data analysis was reviewed and entered into results data.micronsMEAN
OTHER_PRE_SPECIFIEDProportion of Eyes Demonstrating a Reduction in Subretinal Fluid on OCTBaseline and Month 2Significant acute data collection missing therefore only chronic arm data analysis was reviewed and entered into results data.EyesCOUNT_OF_UNITS

Results by group10

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Mean Change in Maximal Subretinal Fluid Height Based on Spectral Domain Optical Coherence Tomography (OCT) Measurement.25mg Eplerenone- Chronic CSCR DiagnosisBaseline139.3Standard Deviation 58.7microns
Mean Change in Maximal Subretinal Fluid Height Based on Spectral Domain Optical Coherence Tomography (OCT) Measurement.Placebo- Chronic CSCR DiagnosisBaseline135.9Standard Deviation 21.8microns
Mean Change in Maximal Subretinal Fluid Height Based on Spectral Domain Optical Coherence Tomography (OCT) Measurement.25mg Eplerenone- Chronic CSCR DiagnosisMonth 251.8Standard Deviation 52.2microns
Mean Change in Maximal Subretinal Fluid Height Based on Spectral Domain Optical Coherence Tomography (OCT) Measurement.Placebo- Chronic CSCR DiagnosisMonth 2172.3Standard Deviation 88.8microns
Mean Change in Subfoveal Fluid Height Based on OCT Measurement25mg Eplerenone- Chronic CSCR DiagnosisBaseline121.4Standard Deviation 75.0microns
Mean Change in Subfoveal Fluid Height Based on OCT MeasurementPlacebo- Chronic CSCR DiagnosisBaseline92.1Standard Deviation 47.4microns
Mean Change in Subfoveal Fluid Height Based on OCT Measurement25mg Eplerenone- Chronic CSCR DiagnosisMonth 229.4Standard Deviation 34.0microns
Mean Change in Subfoveal Fluid Height Based on OCT MeasurementPlacebo- Chronic CSCR DiagnosisMonth 2134.0Standard Deviation 105.9microns
Proportion of Eyes Demonstrating a Reduction in Subretinal Fluid on OCT25mg Eplerenone- Chronic CSCR Diagnosis11Eyes
Proportion of Eyes Demonstrating a Reduction in Subretinal Fluid on OCTPlacebo- Chronic CSCR Diagnosis1Eyes

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTED25mg Eplerenone- Chronic CSCR Diagnosis12
Overall StudySTARTEDPlacebo- Chronic CSCR Diagnosis6
Overall StudyCOMPLETED25mg Eplerenone- Chronic CSCR Diagnosis10
Overall StudyCOMPLETEDPlacebo- Chronic CSCR Diagnosis5
Overall StudyNOT COMPLETED25mg Eplerenone- Chronic CSCR Diagnosis2
Overall StudyNOT COMPLETEDPlacebo- Chronic CSCR Diagnosis1

Adverse events2

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherDizzinessGeneral disorders25mg Eplerenone- Chronic CSCR Diagnosis1121
otherDizzinessGeneral disordersPlacebo- Chronic CSCR Diagnosis060

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortality25mg Eplerenone- Chronic CSCR Diagnosis012
Total, all-cause mortalityPlacebo- Chronic CSCR Diagnosis06
Total, other adverse events25mg Eplerenone- Chronic CSCR Diagnosis112
Total, other adverse eventsPlacebo- Chronic CSCR Diagnosis06
Total, serious adverse events25mg Eplerenone- Chronic CSCR Diagnosis012
Total, serious adverse eventsPlacebo- Chronic CSCR Diagnosis06

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
40522203DERIVED

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons2

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource
25mg Eplerenone- Chronic CSCR Diagnosis vs Placebo- Chronic CSCR Diagnosis: deaths from any causeTrial comparisons
25mg Eplerenone- Chronic CSCR Diagnosis vs Placebo- Chronic CSCR Diagnosis: serious adverse eventsTrial comparisons

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT01990677

GET https://conductscience.org/api/trials/v1/NCT01990677/registered