Post-marketing Safety Study to Assess the Risk of Spontaneous Abortion Following Administration of CERVARIX in the United States and Canada

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Record identity and dates

Source

ClinicalTrials.gov

Source record ID

NCT01290393

Title field or adapter rule

protocolSection.identificationModule.officialTitle

Ingested At

2026-04-28T10:36:51.965537+00:00

Published At

2018-07-26T00:00:00+00:00

Record Updated At

2018-07-26

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, Papillomavirus"]

protocolSection.statusModule.lastUpdatePostDateStruct.date

"2018-07-26"

protocolSection.identificationModule.nctId

"NCT01290393"

protocolSection.identificationModule.officialTitle

"Post-marketing Safety Study to Assess the Risk of Spontaneous Abortion Following Administration of CERVARIX in the United States and Canada"

protocolSection.statusModule.overallStatus

"TERMINATED"

protocolSection.designModule.phases

[]

protocolSection.statusModule.resultsFirstPostDateStruct.date

""

Study condition terms

• Infections, Papillomavirus (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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