CLINICAL_TRIALS ClinicalTrials.gov record update

A Randomized Controlled Trial of Sublingual Misoprostol in Addition to Routine Uterotonics to Reduce Primary Postpartum Haemorrhage in Low Risk Women After Vaginal Delivery

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

Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT05079061
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:38:46.994352+00:00
Published At: 2022-03-03T00:00:00+00:00
Record Updated At: 2022-03-03
Timestamp Basis: source retrieval time was not retained by the feed adapter
Date limitation: source retrieval time was not retained by the feed adapter

protocolSection.conditionsModule.conditions: ["Primary Postpartum Hemorrhage", "Misoprostol", "Delivery Complication"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2022-03-03"
protocolSection.identificationModule.nctId: "NCT05079061"
protocolSection.identificationModule.officialTitle: "A Randomized Controlled Trial of Sublingual Misoprostol in Addition to Routine Uterotonics to Reduce Primary Postpartum Haemorrhage in Low Risk Women After Vaginal Delivery"
protocolSection.statusModule.overallStatus: "UNKNOWN"
protocolSection.designModule.phases: ["PHASE4"]
protocolSection.statusModule.resultsFirstPostDateStruct.date: ""

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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