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CLINICAL_TRIALS ClinicalTrials.gov record update

A 6-Month, Randomized, Open-Label, Active-Comparator Controlled, Parallel-Group Study With a 6-Month Extension to Evaluate the Safety and Efficacy of Alendronate Sodium 70 mg/Vitamin D3 5600 I.U. Combination Tablets Versus Calcitriol in the Treatment of Osteoporosis in Postmenopausal Women in China

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT01350934
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-25T22:26:26.013476+00:00
Published At
2014-07-22T00:00:00+00:00
Record Updated At
2024-06-20
Results Posted At
2014-07-22
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
["Osteoporosis, Postmenopausal"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2024-06-20"
protocolSection.identificationModule.nctId
"NCT01350934"
protocolSection.identificationModule.officialTitle
"A 6-Month, Randomized, Open-Label, Active-Comparator Controlled, Parallel-Group Study With a 6-Month Extension to Evaluate the Safety and Efficacy of Alendronate Sodium 70 mg/Vitamin D3 5600 I.U. Combination Tablets Versus Calcitriol in the Treatment of Osteoporosis in Postmenopausal Women in China"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["PHASE4"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
"2014-07-22"

Study condition terms

  • Osteoporosis, Postmenopausal (protocolSection.conditionsModule.conditions)

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