Clin2
NCT06285409Possibly a fitRecruiting

Uterus contraction medicine study during planned C-sections

Postpartum Hemorrhage

Treatments studied

Part of Women’s health & pregnancy clinical trials.

This study looks at how well different doses of a contraction medicine work after an initial dose in women having a planned C-section. It may help find the best way to prevent bleeding after birth.

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

Phase
N/A
Enrollment
32 people
Ages
18 years to 45 years
Study type
Interventional

Who can take part

  • You are between 37 and 41 weeks pregnant
  • You are not in labor and have not received oxytocin (a labor-inducing medicine)
  • You are having a planned first or second C-section under spinal anesthesia
  • You have not had any other uterine surgery or more than one previous C-section
  • You do not have placenta accreta (a condition where the placenta grows too deeply into the uterus)
  • You are not taking certain medicines like insulin, nifedipine, labetalol, or magnesium sulfate

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.

Similar studies

Other trials that look related to this one.

NCT06285396Recruiting
Diabetes and medication effects on uterine muscle during C-section

This trial studies how three medications (ephedrine, phenylepinephrine, and norepinephrine) affect the contraction strength of uterine muscle tissue from pregnant people with type 2 or gestational diabetes during planned C-sections. It aims to understand if these drugs act differently in people with diabetes, which could help tailor safer treatments for low blood pressure during surgery.

Toronto, Ontario
NCT05290129Recruiting
Oxytocin drip during C-section labor to help maintain contractions

This trial tests whether a continuous oxytocin infusion during a C-section helps maintain labor progress in people already receiving oxytocin. It may help reduce labor-related complications, but only if you meet the safety requirements for anesthesia and pregnancy conditions.

Toronto, Ontario
NCT07636421Recruiting· Phase 4
Comparing two medications to prevent bleeding after planned C-section

This trial tests two medicines given during a planned C-section to see which is better at preventing heavy bleeding. It may help make delivery safer for healthy women having a scheduled cesarean.

Buraidah, Al-Qassim Region
NCT07353281Not yet recruiting
Preventing heavy bleeding after vaginal birth: comparing two medicines

This study compares two medications given right after vaginal delivery to prevent heavy bleeding (postpartum hemorrhage). The goal is to find which one works better for women who have a higher risk of bleeding after childbirth.

NCT07188207Not yet recruiting
Rectal misoprostol to reduce bleeding during planned cesarean section

This study tests whether giving a medication (misoprostol) rectally during a planned C-section can help reduce blood loss after delivery. It may help women have a safer recovery with less bleeding.

NCT07688512Not yet recruiting· Phase 4
Oxytocin dosing for women at risk of bleeding after C-section

This study compares two ways of giving the medicine oxytocin (which helps the womb tighten to reduce bleeding) after a C-section in women at high risk for heavy bleeding. It will see if giving it as a single injection or as a slow drip works better at preventing excessive blood loss.

Hear when a new Postpartum Hemorrhage trial opens

We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.