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CLINICAL_TRIALS ClinicalTrials.gov record update

Phase 3b, Multicenter, Randomized, Single-blind, Parallel Group Trial of the Effects of Titrated Oral SAMSCA(r) (Tolvaptan) 15, 30, or 60 mg QD Compared to Placebo Plus Fluid Restriction on Length of Hospital Stay and Symptoms in Subjects Hospitalized With Dilutional Hyponatremia

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT01227512
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:35:49.279681+00:00
Published At
2014-10-17T00:00:00+00:00
Record Updated At
2014-10-30
Results Posted At
2014-10-17
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", "Dilutional Hyponatremia", "Inappropriate ADH Syndrome"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2014-10-30"
protocolSection.identificationModule.nctId
"NCT01227512"
protocolSection.identificationModule.officialTitle
"Phase 3b, Multicenter, Randomized, Single-blind, Parallel Group Trial of the Effects of Titrated Oral SAMSCA(r) (Tolvaptan) 15, 30, or 60 mg QD Compared to Placebo Plus Fluid Restriction on Length of Hospital Stay and Symptoms in Subjects Hospitalized With Dilutional Hyponatremia"
protocolSection.statusModule.overallStatus
"TERMINATED"
protocolSection.designModule.phases
["PHASE3"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
"2014-10-17"

Study condition terms

  • Hyponatremia (protocolSection.conditionsModule.conditions)
  • Dilutional Hyponatremia (protocolSection.conditionsModule.conditions)
  • Inappropriate ADH Syndrome (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.