Coagulation Profile Surrounding Normal Cesarean Delivery

NCT02482246 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 10

Last updated 2015-12-02

No results posted yet for this study

Summary

Healthy parturients presenting for scheduled cesarean delivery will have blood drawn and measured for microparticles at baseline, immediately after delivery, and at several time points thereafter.

Conditions

  • Pregnancy

Sponsors & Collaborators

  • University of Chicago

    lead OTHER

Eligibility

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

Timeline & Regulatory

Start
2014-01-31
Primary Completion
2014-12-31
Completion
2015-06-30

Countries

  • United States

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 NCT02482246 on ClinicalTrials.gov