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CLINICAL_TRIALS ClinicalTrials.gov record update

Foundation Fighting Blindness My Retina Tracker Registry

This page presents selected fields from the linked source record. It does not add a medical interpretation.

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT02435940
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-25T22:26:42.033661+00:00
Published At
2025-03-27T00:00:00+00:00
Record Updated At
2025-03-27
Timestamp Basis
source retrieval time was not retained by the feed adapter
Date limitation
source retrieval time was not retained by the feed adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions
["Eye Diseases Hereditary", "Retinal Disease", "Achromatopsia", "Bardet-Biedl Syndrome", "Bassen-Kornzweig Syndrome", "Batten Disease", "Best Disease", "Choroidal Dystrophy", "Choroideremia", "Cone Dystrophy", "Cone-Rod Dystrophy", "Congenital Stationary Night Blindness", "Enhanced S-Cone Syndrome", "Fundus Albipunctatus", "Goldmann-Favre Syndrome", "Gyrate Atrophy", "Juvenile Macular Degeneration", "Kearns-Sayre Syndrome", "Leber Congenital Amaurosis", "Refsum Syndrome", "Retinitis Pigmentosa", "Retinitis Punctata Albescens", "Retinoschisis", "Rod-Cone Dystrophy", "Rod Dystrophy", "Rod Monochromacy", "Stargardt Disease", "Usher Syndrome"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2025-03-27"
protocolSection.identificationModule.nctId
"NCT02435940"
protocolSection.identificationModule.officialTitle
"Foundation Fighting Blindness My Retina Tracker Registry"
protocolSection.statusModule.overallStatus
"RECRUITING"
protocolSection.designModule.phases
[]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Eye Diseases Hereditary (protocolSection.conditionsModule.conditions)
  • Retinal Disease (protocolSection.conditionsModule.conditions)
  • Achromatopsia (protocolSection.conditionsModule.conditions)
  • Bardet-Biedl Syndrome (protocolSection.conditionsModule.conditions)
  • Bassen-Kornzweig Syndrome (protocolSection.conditionsModule.conditions)
  • Batten Disease (protocolSection.conditionsModule.conditions)
  • Best Disease (protocolSection.conditionsModule.conditions)
  • Choroidal Dystrophy (protocolSection.conditionsModule.conditions)
  • Choroideremia (protocolSection.conditionsModule.conditions)
  • Cone Dystrophy (protocolSection.conditionsModule.conditions)
  • Cone-Rod Dystrophy (protocolSection.conditionsModule.conditions)
  • Congenital Stationary Night Blindness (protocolSection.conditionsModule.conditions)
  • Enhanced S-Cone Syndrome (protocolSection.conditionsModule.conditions)
  • Fundus Albipunctatus (protocolSection.conditionsModule.conditions)
  • Goldmann-Favre Syndrome (protocolSection.conditionsModule.conditions)
  • Gyrate Atrophy (protocolSection.conditionsModule.conditions)
  • Juvenile Macular Degeneration (protocolSection.conditionsModule.conditions)
  • Kearns-Sayre Syndrome (protocolSection.conditionsModule.conditions)
  • Leber Congenital Amaurosis (protocolSection.conditionsModule.conditions)
  • Refsum Syndrome (protocolSection.conditionsModule.conditions)
  • Retinitis Pigmentosa (protocolSection.conditionsModule.conditions)
  • Retinitis Punctata Albescens (protocolSection.conditionsModule.conditions)
  • Retinoschisis (protocolSection.conditionsModule.conditions)
  • Rod-Cone Dystrophy (protocolSection.conditionsModule.conditions)
  • Rod Dystrophy (protocolSection.conditionsModule.conditions)
  • Rod Monochromacy (protocolSection.conditionsModule.conditions)
  • Stargardt Disease (protocolSection.conditionsModule.conditions)
  • Usher Syndrome (protocolSection.conditionsModule.conditions)

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.