CLINICAL_TRIALS ClinicalTrials.gov record update

Multicenter and Prospective Study to Determine the Satisfaction With Actonel (Risedronate Sodium) 35mg Once a Week Using Biochemical Markers of Bone as a Control, in Postmenopausal Women With Osteoporosis

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT00632216
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:34:52.058465+00:00
Published At: 2008-03-11T00:00:00+00:00
Record Updated At: 2008-03-11
Timestamp Basis: source retrieval time was not retained by the feed adapter
Date limitation: source retrieval time was not retained by the feed adapter

protocolSection.conditionsModule.conditions: ["Osteoporosis, Postmenopausal"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2008-03-11"
protocolSection.identificationModule.nctId: "NCT00632216"
protocolSection.identificationModule.officialTitle: "Multicenter and Prospective Study to Determine the Satisfaction With Actonel (Risedronate Sodium) 35mg Once a Week Using Biochemical Markers of Bone as a Control, in Postmenopausal Women With Osteoporosis"
protocolSection.statusModule.overallStatus: "COMPLETED"
protocolSection.designModule.phases: ["PHASE4"]
protocolSection.statusModule.resultsFirstPostDateStruct.date: ""

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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