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CLINICAL_TRIALS ClinicalTrials.gov record update

A Multicenter, Randomized, Open-label, Active-controlled Study to Assess the Impact of Auryxia (Ferric Citrate) on Erythropoiesis-Stimulating Agent (ESA) Use, Intravenous (IV) Iron Use, Phosphate Control, and Anemia Control in Adult Participants on In-Center Hemodialysis or Home Dialysis

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT04922645
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:38:55.238631+00:00
Published At
2022-11-07T00:00:00+00:00
Record Updated At
2022-11-07
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
["Hyperphosphatemia", "Anemia, Iron Deficiency", "Renal Insufficiency"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2022-11-07"
protocolSection.identificationModule.nctId
"NCT04922645"
protocolSection.identificationModule.officialTitle
"A Multicenter, Randomized, Open-label, Active-controlled Study to Assess the Impact of Auryxia (Ferric Citrate) on Erythropoiesis-Stimulating Agent (ESA) Use, Intravenous (IV) Iron Use, Phosphate Control, and Anemia Control in Adult Participants on In-Center Hemodialysis or Home Dialysis"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["PHASE4"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Hyperphosphatemia (protocolSection.conditionsModule.conditions)
  • Anemia, Iron Deficiency (protocolSection.conditionsModule.conditions)
  • Renal Insufficiency (protocolSection.conditionsModule.conditions)

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

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