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Trial · NCT02390284

Stop Retinal Ganglion Cell Dysfunction Study

NCT02390284, Phase 3, Terminated, University of Miami; results first posted 2025-08-26

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Stop Retinal Ganglion Cell Dysfunction Study. Trials, record NCT02390284. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02390284

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Trial

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

Title
Stop Retinal Ganglion Cell Dysfunction Study
NCT number
NCT02390284
Status
Terminated
Phases
Phase 3
Enrollment
28 participants, actual
Lead sponsor
University of Miami
Conditions
Glaucoma
Interventions
Latanoprost, Bimatoprost, Travoprost, Timolol, Dorzolamide, Brinzolamide, Acetazolamide, Methazolamide
First posted
2015-03-17
Last updated
2025-08-26
Results first posted
2025-08-26
Limitations and caveats
Early termination leading to small numbers of subjects analyzed and qualifying for the study.

Source ClinicalTrials.gov

Registered outcomes3

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

ListOutcomeTime frameDescription
PrimaryRetinal Nerve Fiber Layer ThicknessBaselineAs measured by Optical Coherence Tomography in different timepoints as an absolute value in micrometers.
SecondaryPattern Electroretinogram AmplitudeBaselineAssessed via Pattern Electroretinogram in nanovolts
SecondaryPattern Electroretinogram PhaseBaselineAssessed via Pattern Electroretinogram in degrees

Outcomes3

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYRetinal Nerve Fiber Layer ThicknessBaselineNo patients had abnormal PERG and could not be included in the first two arms from the baseline timepoint, only baseline measurements could be included.micrometersMEAN
SECONDARYPattern Electroretinogram AmplitudeBaselineNo patients had abnormal PERG and could not be included in the first two arms from the baseline timepoint, only baseline measurements could be included.nanovoltsMEAN
SECONDARYPattern Electroretinogram PhaseBaselineNo patients had abnormal PERG and could not be included in the first two arms from the baseline timepoint, only baseline measurements could be included.degreesMEAN

Results by group3

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

OutcomeGroupCategoryValueSpreadUnits
Retinal Nerve Fiber Layer ThicknessNormal79Full Range 76 to 89micrometers
Pattern Electroretinogram AmplitudeNormal706Full Range 455 to 1344nanovolts
Pattern Electroretinogram PhaseNormal67.34Full Range 22 to 96degrees

Participant flow9

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDAbnormal PERG Untreated0
Overall StudySTARTEDAbnormal PERG Treated0
Overall StudySTARTEDNormal28
Overall StudyCOMPLETEDAbnormal PERG Untreated0
Overall StudyCOMPLETEDAbnormal PERG Treated0
Overall StudyCOMPLETEDNormal19
Overall StudyNOT COMPLETEDAbnormal PERG Untreated0
Overall StudyNOT COMPLETEDAbnormal PERG Treated0
Overall StudyNOT COMPLETEDNormal9

Adverse events0

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

None in this release.

Adverse event totals9

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityAbnormal PERG Untreated00
Total, all-cause mortalityAbnormal PERG Treated00
Total, all-cause mortalityNormal028
Total, other adverse eventsAbnormal PERG Untreated00
Total, other adverse eventsAbnormal PERG Treated00
Total, other adverse eventsNormal028
Total, serious adverse eventsAbnormal PERG Untreated00
Total, serious adverse eventsAbnormal PERG Treated00
Total, serious adverse eventsNormal028

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants1

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.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal years
R01EY014957Reversible Dysfunction of Retinal Ganglion Cells in GlaucomaPORCIATTI, VITTORIOUNIVERSITY OF MIAMI SCHOOL OF MEDICINENATIONAL EYE INSTITUTE2005 to 2017

Trial comparisons0

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

None in this release.

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/NCT02390284

GET https://conductscience.org/api/trials/v1/NCT02390284/registered