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Clinical Trial Summary

Post partum haemorrhage is a concerning situation in maternity wards, though it is not the first cause of maternal mortality anymore. It has been already shown that low fibrinogen level is a major predictive factor of massive bleeding after delivery. In this situation, the early knowledge of fibrinogen level could enhance care of women experiencing post partum haemorrhage. In a cohort of women suffering from post partum haemorrhage, this study will evaluate whether assessing fibrinogen level would be faster using the Quantra® system than the standard coagulation test.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05336838
Study type Observational
Source University Hospital, Montpellier
Contact Jessie Grenié, MD
Phone 00330467336472
Email j-grenie@chu-montpellier.fr
Status Not yet recruiting
Phase
Start date May 1, 2022
Completion date May 1, 2023

See also
  Status Clinical Trial Phase
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Recruiting NCT00344929 - Severe Post Partum Haemorrhage (PPH): A Randomized Trial on Transversal Intervention in 6 French Perinatal Networks N/A
Completed NCT02775773 - Clinical Study to Assess the Equivalence of Tranexamic Acid vs Oxytocin in Reducing the PPH Phase 3
Completed NCT02216383 - Intramuscular Oxytocics: A Randomised Control Trial Phase 3
Completed NCT01571323 - Combined Use of Oxytocin and Misoprostol Versus Oxytocin Infusion and Misoprostol Alone to Reduce Blood Loss at Cesarean Section Phase 1/Phase 2
Terminated NCT02908126 - Compare Efficacy of Oxytocin Administrations on Postpartum Uterine Contractility Phase 1
Terminated NCT02900690 - Health Economics Evaluation of the Management of Severe Postpartum Hemorrhage: Comparison of Recombinant Activated Factor VII Strategy to the Reference Strategy