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CLINICAL_TRIALS ClinicalTrials.gov record update

Factors and Outcomes Associated With Use of Cabergoline Among Postpartum Women in Israel

This page presents selected fields from the linked source record. It does not add a medical interpretation.

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT03965572
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:38:29.107713+00:00
Published At
2021-09-28T00:00:00+00:00
Record Updated At
2021-09-28
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
["Lactation Suppressed", "Cabergoline Adverse Reaction", "Postpartum DVT", "Postpartum Depression"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2021-09-28"
protocolSection.identificationModule.nctId
"NCT03965572"
protocolSection.identificationModule.officialTitle
"Factors and Outcomes Associated With Use of Cabergoline Among Postpartum Women in Israel"
protocolSection.statusModule.overallStatus
"UNKNOWN"
protocolSection.designModule.phases
[]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Lactation Suppressed (protocolSection.conditionsModule.conditions)
  • Cabergoline Adverse Reaction (protocolSection.conditionsModule.conditions)
  • Postpartum DVT (protocolSection.conditionsModule.conditions)
  • Postpartum Depression (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.