Clin2
NCT07019623Possibly a fitRecruiting

U-CaVIT device vs standard care for preventing heavy bleeding after c-section

Postpartum Hemorrhage (Primary)HemorrhagePostpartum ComplicationDelivery ,Complications,MaternalPregnancy ComplicationsCesarean DeliveryBalloon

Part of Women’s health & pregnancy clinical trials.

This study tests a new device called U-CaVIT to prevent heavy bleeding after a planned cesarean delivery in women at high risk. It compares the U-CaVIT device to standard care to see which works better.

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

Phase
N/A
Enrollment
70 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You are 18 years or older
  • You are at least 30 weeks pregnant on the day of delivery
  • Your pregnancy is ongoing (vital)
  • You are scheduled for a planned cesarean delivery (not an emergency)
  • You have at least one risk factor for heavy bleeding: previous heavy bleeding, obesity (BMI 30+), 4 or more previous births, age 45+, multiple pregnancy, too much amniotic fluid, or a suspected large baby (≥4500g)
  • You are not participating in another research study and can understand English or German

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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