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Postpartum Ultrasound Evaluation to Assess Risk of Hemorrhage

Endeavor Health · NCT06898034

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 17+ · Women only
Healthy volunteers
Accepted
Study type
Observational
Target enrollment
1725
US sites recruiting
1
Study start
March 10, 2025
Record last updated
March 27, 2025

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

Up to 5% of patients in the United States have a postpartum hemorrhage. "Postpartum hemorrhage" means excessive bleeding after delivery. The majority of these bleeds occur immediately with delivery.

The current study focuses on hemorrhages that occur in the "medium-term" (1.5-24 hours after delivery). Investigators are examining whether ultrasound exams performed at the beginning of this period 1.5 to 2 hours after birth can identify markers that predict a medium-term bleed. Data collected for this study will include medical and obstetrical history, details about the course and outcomes of patients' labor and delivery, and particulars about postpartum bleeding. This information will be collected through the end of the patients' delivery admission and will allow correlation with the results of the ultrasound exam. If patients are re-admitted to the hospital after the delivery discharge, investigators may also collect relevant information about those admissions up to 6 weeks postpartum.

All patients after term delivery (≥ 37 weeks' gestation) will be eligible to participate. Patients will be approached to provide consent for participation as early as feasible during a prenatal visit (≥ 36 weeks' gestation) or during the delivery admission. No subjects will be consented while in significant pain, >6cm dilated without an epidural, or >8cm dilatated with an epidural.

Being studied: Ultrasound

Conditions: Pregnancy Related; Post Partum Hemorrhage

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

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

Recruiting US locations

  • Endeavor Health

    Evanston, IL 60201

    Site contact: Emmet Hirsch, MD · EHirsch@northshore.org

Study contacts (from the official record)

  • Kate Honeyfield · 847-570-2243 · KHoneyfield@northshore.org
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Postpartum Ultrasound Evaluation to Assess Risk of Hemorrhage (NCT06898034) | Bored Studies