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A Prospective and Randomized Study of Efficacy and Safety of Transdermal Oxybutynin Versus Oral Oxybutynin in The Management of Children With Overactive Bladder

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT07081906
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-25T22:27:33.951043+00:00
Published At
2025-07-23T00:00:00+00:00
Record Updated At
2025-07-23
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
["Overactive Bladder (OAB)", "Drug Delivery Systems", "Anticholinergic Side Effects", "Children and Adolescents, Boys and Girls"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2025-07-23"
protocolSection.identificationModule.nctId
"NCT07081906"
protocolSection.identificationModule.officialTitle
"A Prospective and Randomized Study of Efficacy and Safety of Transdermal Oxybutynin Versus Oral Oxybutynin in The Management of Children With Overactive Bladder"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["NA"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Overactive Bladder (OAB) (protocolSection.conditionsModule.conditions)
  • Drug Delivery Systems (protocolSection.conditionsModule.conditions)
  • Anticholinergic Side Effects (protocolSection.conditionsModule.conditions)
  • Children and Adolescents, Boys and Girls (protocolSection.conditionsModule.conditions)

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.