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A Phase III, Double-Blind, Randomized, Placebo-Controlled, Multi-Center, Dose-Titration Study to Assess the Efficacy, Safety and Pharmacokinetics of Intravenous Conivaptan (Vaprisol®) in Pediatric Subjects With Euvolemic or Hypervolemic Hyponatremia

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT01451411
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:35:59.029817+00:00
Published At
2016-03-01T00:00:00+00:00
Record Updated At
2016-03-01
Results Posted At
2016-03-01
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
["Hyponatremia"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2016-03-01"
protocolSection.identificationModule.nctId
"NCT01451411"
protocolSection.identificationModule.officialTitle
"A Phase III, Double-Blind, Randomized, Placebo-Controlled, Multi-Center, Dose-Titration Study to Assess the Efficacy, Safety and Pharmacokinetics of Intravenous Conivaptan (Vaprisol\u00ae) in Pediatric Subjects With Euvolemic or Hypervolemic Hyponatremia"
protocolSection.statusModule.overallStatus
"TERMINATED"
protocolSection.designModule.phases
["PHASE3"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
"2016-03-01"

Study condition terms

  • Hyponatremia (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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