Study of Biological Determinants of Bleeding Postpartum (HPP-IPF)

Regional University Hospital Center (CHRU)

Status: Completed

Conditions: Postpartum Hemorrhage

Study type: Observational

Funder types: Other

Identifiers

NCT02884804

HPP-IPF (RB 11.080)

Details and patient eligibility

About

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.

Enrollment: 3,599 patients

Sex: Female

Volunteers: No Healthy Volunteers

Inclusion criteria

• Woman giving birth in a maternity of Finistère

Exclusion criteria

• Refuse to participate in the study