Study of Coagulation Activation Markers and Pre Eclampsia

NCT01261351 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2014-12-18

No results posted yet for this study

Summary

The primary purpose of the trial is to evaluate coagulation activator markers in patients with pre eclampsia compared to control (normal pregnancy) and to correlate these markers with the severity of the pathology.

Conditions

  • Pre Eclampsia

Sponsors & Collaborators

  • University Hospital, Lille

    lead OTHER

Principal Investigators

  • Véronique Houfflin Debarge, PHD · Universituy Hospital Of Lille, France

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-05-31
Primary Completion
2014-06-30
Completion
2014-06-30

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 NCT01261351 on ClinicalTrials.gov