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A Phase III, Randomised, Open-Label, Comparative Study of Intravenous Iron Isomaltoside 1000 (Monofer®) and Iron Sucrose in Subjects With Iron Deficiency Anaemia and Who Are Intolerant or Unresponsive to Oral Iron Therapy or Who Need Iron Rapidly (PROVIDE)

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT02130063
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:37:08.390372+00:00
Published At
2018-05-22T00:00:00+00:00
Record Updated At
2018-09-27
Results Posted At
2018-05-22
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
["Iron Deficiency Anaemia"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2018-09-27"
protocolSection.identificationModule.nctId
"NCT02130063"
protocolSection.identificationModule.officialTitle
"A Phase III, Randomised, Open-Label, Comparative Study of Intravenous Iron Isomaltoside 1000 (Monofer\u00ae) and Iron Sucrose in Subjects With Iron Deficiency Anaemia and Who Are Intolerant or Unresponsive to Oral Iron Therapy or Who Need Iron Rapidly (PROVIDE)"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["PHASE3"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
"2018-05-22"

Study condition terms

  • Iron Deficiency Anaemia (protocolSection.conditionsModule.conditions)

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