Clinical Trials Directory

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UnknownNCT05336838

Improving Management of Post-partum Haemorrhage With Quantra® System

Use of Quantra® System in Clinical Practice to Improve Management of Post-partum Haemorrhage : a Prospective Study

Status
Unknown
Phase
Study type
Observational
Enrollment
60 (estimated)
Sponsor
University Hospital, Montpellier · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Timeline

Start date
2022-05-01
Primary completion
2023-05-01
Completion
2023-05-01
First posted
2022-04-20
Last updated
2022-04-20

Source: ClinicalTrials.gov record NCT05336838. Inclusion in this directory is not an endorsement.