CompletedNot Applicable

Thromboelastography in Non-elective Cesarean Delivery

United States33 participantsStarted 2011-08

Plain-language summary

The purpose of the study is to assess the coagulation changes that occur in laboring patients undergoing non-elective (intrapartum)Cesarean delivery using thromboelastography (TEG). We will compare coagulation data to assess potential coagulation changes associated with hemoglobin changes before and after surgery, and related to estimated blood loss.

Who can participate

Age range

18 Years – 40 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Obstetric in-patients * Laboring patients with Epidurals for Labor Analgesia going for non-elective Cesarean * Patients of all ethnic backgrounds will be included * Singleton pregnancy * ASA 1 or 2 Exclusion Criteria: * Patients with underlying coagulation disorders. * Patients with thrombocytopenia (platelet count \<100). * Patients with pregnancy-induced hypertension, pre-eclampsia. * Patients requiring the following medications prior to surgery: NSAIDS, aspirin, anticoagulants. * Patients requiring elective Cesarean delivery. * Patients with significant obstetric or medical disease. * No patients \<18 years of age will be recruited.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Estimated blood loss; Coagulation data (Thromboelastography, Laboratory)

Timeframe: pre and post cesarean delivery, an expected average of 75 minutes

Trial details

NCT IDNCT01514591

SponsorStanford University

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2013-06

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