Coagulation Profile Surrounding Normal Cesarean Delivery

Completed

Conditions studied: Pregnancy

In brief

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.

Key facts

Study ID

NCT02482246

Run by

University of Chicago

People needed

10

Starts

2014-01-01

Expected to finish

2015-06-01

Last updated by the study team

2015-12-02

Who can join

Age: 18 and older, up to 60. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• All patients with a singleton pregnancy with gestational age greater than or equal to 36 weeks who present for scheduled cesarean delivery will be eligible for participation.

You may not qualify if…

• Specific exclusion criteria include emergency cesarean delivery, labor pain, hypertensive diseases of pregnancy, diabetes, known placental abnormalities such as placental abruption, placenta previa and placenta accreta, and known disorders of coagulation or recent anticoagulant therapy.

Where it is running

• University of Chicago — Chicago, Illinois, United States

Full record on ClinicalTrials.gov

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