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NCT03591679

Bilateral Uterine Artery Ligation in Reducing Incidence of Postpartum Hemorrhage in Cesarean Section

Completed NA Last updated 11 March 2019
What this trial tests

NA trial testing Oxytocin in Post Partum Hemorrhage in 1,070 participants. Completed in 1 January 2019.

Timeline
1 December 2017
Primary endpoint
30 November 2018
1 January 2019

Quick facts

Lead sponsorAssiut University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment1,070
Start date1 December 2017
Primary completion30 November 2018
Estimated completion1 January 2019
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Assiut University

Who can join

Eligibility, female only, with Post Partum Hemorrhage. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The patients were recruited from women attending labor ward to undergo cesarean section.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Randomized controlled trial of the effect of bilateral uterine artery ligation during cesarean among women at risk of uterine atony.
    Samy A, Ali MK, Abbas AM, Wahab HA, et al · · 2020 · PMID 31755559 · DOI 10.1002/ijgo.13064

Verify or expand the search:

Other trials of Oxytocin

Trials testing the same drug.

Other recruiting trials for Post Partum Hemorrhage

Currently open trials in the same condition.

Other Assiut University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03591679.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing