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Clinical Trial Summary

This study concerns women diagnosed with postpartum hemorrhage and requiring sulprostone therapy. Included patients are randomized to two arms: the "Sulprostone + Bakri balloon" arm versus the "Sulprostone alone" arm.

The main objective of this study is to compare the efficiency of a care strategy including the Bakri balloon to that of routine care without the Bakri balloon via a cost-consequence study juxtaposing costs and the necessity of invasive procedures (arterial embolization, ligation of arteries, hysterectomy, intrauterine sutures) for controlling postpartum hemorrhage.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01980173
Study type Interventional
Source Centre Hospitalier Universitaire de Nimes
Contact
Status Terminated
Phase N/A
Start date September 5, 2014
Completion date March 30, 2017

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