Evaluating ultrasound to predict postpartum hemorrhage risk

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study investigates the use of ultrasound exams performed 1.5 to 2 hours after delivery to identify markers that may predict the risk of medium-term postpartum hemorrhage, which occurs between 1.5 to 24 hours post-delivery. The study will collect data on patients' medical and obstetrical history, labor and delivery outcomes, and details about postpartum bleeding. This information will be correlated with ultrasound results to enhance understanding of bleeding risks in postpartum patients. The goal is to improve early identification and management of potential hemorrhage.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Currently pregnant and planning to deliver at Endeavor Health \>37 weeks gestational age
* English speaking
* Labor \<6cm dilated at time of consent without epidural
* Labor \<8cm dilated at time of consent with epidural

Exclusion Criteria:

* Preterm delivery
* Non-English speaking
* Any conditions that impairs potential participants decision making

Where it's running

• Endeavor Health
  Evanston, Illinois, United States Recruiting

Study contacts

• Study coordinator: Kate Honeyfield
• Email: KHoneyfield@northshore.org
• Phone: 847-570-2243

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.