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CLINICAL_TRIALS ClinicalTrials.gov record update

A One-Year, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Determine the Efficacy and Safety of 35-mg Risedronate Administered Once a Week in the Prevention of Osteoporosis in Postmenopausal Women

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT00402441
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:34:59.337545+00:00
Published At
2009-04-29T00:00:00+00:00
Record Updated At
2009-04-29
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
"2009-04-29"
protocolSection.identificationModule.nctId
"NCT00402441"
protocolSection.identificationModule.officialTitle
"A One-Year, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Determine the Efficacy and Safety of 35-mg Risedronate Administered Once a Week in the Prevention of Osteoporosis in Postmenopausal Women"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["PHASE4"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Osteoporosis, Postmenopausal (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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