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CLINICAL_TRIALS ClinicalTrials.gov record update

The Incidence of Hyperfibrinolysis During Vaginal Delivery and Cesarean Section

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
NCT05975112
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:39:53.030435+00:00
Published At
2024-03-21T00:00:00+00:00
Record Updated At
2024-03-21
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
["Hyperfibrinolysis", "Cesarean Section Complications", "Coagulation Defect; Bleeding", "Peripartum Haemorrhage"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2024-03-21"
protocolSection.identificationModule.nctId
"NCT05975112"
protocolSection.identificationModule.officialTitle
"The Incidence of Hyperfibrinolysis During Vaginal Delivery and Cesarean Section"
protocolSection.statusModule.overallStatus
"UNKNOWN"
protocolSection.designModule.phases
[]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Hyperfibrinolysis (protocolSection.conditionsModule.conditions)
  • Cesarean Section Complications (protocolSection.conditionsModule.conditions)
  • Coagulation Defect; Bleeding (protocolSection.conditionsModule.conditions)
  • Peripartum Haemorrhage (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.