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Study of Biological Determinants of Bleeding Postpartum

NCT02884804 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 3599

Last updated 2016-08-31

No results posted yet for this study

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.

Conditions

  • Postpartum Hemorrhage

Sponsors & Collaborators

  • University Hospital, Brest

    lead OTHER

Principal Investigators

  • PAN-PETESCH Brigitte, Dr. · CHRU de BREST

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-11-30
Primary Completion
2015-05-31
Completion
2015-05-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02884804 on ClinicalTrials.gov