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NCT06351969Possibly a fitNot yet recruiting

Predicting blood loss after birth with placenta accreta

Post Partum Hemorrhage

Part of Women’s health & pregnancy clinical trials.

This study uses ultrasound to measure the thickness of the placenta and nearby uterus in pregnant women with a condition called placenta accreta, to see if these measurements can help predict how much bleeding might happen after delivery.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
150 people
Ages
18 years to 50 years
Study type
Observational

Who can take part

  • You must be at least 37 weeks pregnant.
  • You must be carrying only one baby.
  • You cannot have a serious blood disorder that affects clotting.
  • You cannot have had heavy bleeding after a previous pregnancy.
  • You cannot be in labor early (before 37 weeks) or have a baby that has passed away in the womb.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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