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NCT06483724Possibly a fitNot yet recruiting

Comparing two ways to reduce bleeding during c-section for placenta accreta

Placenta Accreta Spectrum

Part of Women’s health & pregnancy clinical trials.

This study compares two methods (a cervical tourniquet and tying off the uterine artery) to control bleeding during a c-section for women with placenta accreta. If you are having an elective c-section at 36 weeks or later for this condition, this trial may help reduce blood loss.

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

Phase
N/A
Enrollment
82 people
Ages
18 years to 38 years
Study type
Interventional

Who can take part

  • You must have been told by ultrasound that you have a condition called placenta accreta (where the placenta grows too deeply into the womb wall).
  • Your pregnancy must be with just one baby, and the baby must be alive.
  • Your scheduled c-section should happen at 36 weeks or later.
  • You cannot have already decided to have your uterus removed (hysterectomy).
  • You cannot have other uterine problems like fibroids or cancer, a bleeding disorder, or severe obesity (BMI over 40).
  • You should not be in labor or have vaginal bleeding before the planned surgery.

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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