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Immunogenicity, Reactogenicity and Safety Study to Evaluate Two Doses of the Lyophilised Formulation of the Human Rotavirus (HRV) Vaccine When Administered to Healthy Korean Infants Previously Uninfected With HRV

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT00969228
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:37:26.777037+00:00
Published At
2011-11-28T00:00:00+00:00
Record Updated At
2020-01-18
Results Posted At
2011-11-28
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
["Infections, Rotavirus", "Rotavirus Vaccines"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2020-01-18"
protocolSection.identificationModule.nctId
"NCT00969228"
protocolSection.identificationModule.officialTitle
"Immunogenicity, Reactogenicity and Safety Study to Evaluate Two Doses of the Lyophilised Formulation of the Human Rotavirus (HRV) Vaccine When Administered to Healthy Korean Infants Previously Uninfected With HRV"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["PHASE4"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
"2011-11-28"

Study condition terms

  • Infections, Rotavirus (protocolSection.conditionsModule.conditions)
  • Rotavirus Vaccines (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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