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CLINICAL_TRIALS ClinicalTrials.gov record update

Open Label, Parallel Group, Multicenter Study of Two Intravenous (IV) Ibandronate Dose Regimens (2 mg Every 2 Months and 3 mg Every 3 Months) in Women With Postmenopausal Osteoporosis Who Completed Trial BM16550

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT00551174
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:35:08.549157+00:00
Published At
2011-05-30T00:00:00+00:00
Record Updated At
2011-07-22
Results Posted At
2011-05-30
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
["Post-Menopausal Osteoporosis"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2011-07-22"
protocolSection.identificationModule.nctId
"NCT00551174"
protocolSection.identificationModule.officialTitle
"Open Label, Parallel Group, Multicenter Study of Two Intravenous (IV) Ibandronate Dose Regimens (2 mg Every 2 Months and 3 mg Every 3 Months) in Women With Postmenopausal Osteoporosis Who Completed Trial BM16550"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["PHASE4"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
"2011-05-30"

Study condition terms

  • Post-Menopausal Osteoporosis (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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