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An Open-Label Multicenter Study to Assess the Efficacy and Safety of Daily Oral Administration of 5 and 10mg VESIcare® (Solifenacin Succinate) in Patients Who Wish to Switch From Detrol LA® (Tolterodine Tartrate Extended Release) for the Treatment of Overactive Bladder Symptoms Versus: VESIcare® Efficacy and Research Study US

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT00454740
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:35:37.866242+00:00
Published At
2014-09-18T00:00:00+00:00
Record Updated At
2014-09-18
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
["Urinary Bladder, Overactive"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2014-09-18"
protocolSection.identificationModule.nctId
"NCT00454740"
protocolSection.identificationModule.officialTitle
"An Open-Label Multicenter Study to Assess the Efficacy and Safety of Daily Oral Administration of 5 and 10mg VESIcare\u00ae (Solifenacin Succinate) in Patients Who Wish to Switch From Detrol LA\u00ae (Tolterodine Tartrate Extended Release) for the Treatment of Overactive Bladder Symptoms Versus: VESIcare\u00ae Efficacy and Research Study US"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["PHASE3"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Urinary Bladder, Overactive (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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