Study of Biological Determinants of Bleeding Postpartum
Completed
- Conditions
- Postpartum Hemorrhage
- Registration Number
- NCT02884804
- Lead Sponsor
- University Hospital, Brest
- Brief Summary
At the entry of the delivery room, a standard blood analysis will be performed (Blood count, PT, aPTT, Fibrinogen, and D-Dimer) for each women (if they are agree), according to the center's practices.
The percentage of the immature platelets is a an additional parameter on the hemogram.
The clinical assessments (recorded in medical records) and biological values will be used to determine if there is a correlation between these data and the occurrence of postpartum hemorrhage.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 3599
Inclusion Criteria
- Woman giving birth in a maternity of Finistère
Exclusion Criteria
- Refuse to participate in the study
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postpartum Hemorrhage Volume of blood loss up to 24 hours after delivery and / or weight compresses collected at delivery, and / or diagnosis of the clinician Percentage of immature platelets Percentage of immature platelets just before the entry in the birth room
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
CHRU de BREST
🇫🇷Brest, France