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
NCT07636421Not yet recruiting· Phase 4
Carbetocin alone versus carbetocin plus oxytocin for scheduled cesarean delivery

This trial compares two medication approaches to prevent excessive bleeding during planned cesarean delivery under spinal anesthesia. Researchers want to see if one medication (carbetocin) works as well as carbetocin combined with a second medication (oxytocin).

Buraidah, Al-Qassim Region
NCT07353281Not yet recruiting
Comparing two drugs to prevent heavy bleeding after childbirth

This trial compares two medications, carbetocin and misoprostol, to see which works better at preventing heavy bleeding (postpartum hemorrhage) after a vaginal delivery. It is for women who have one or more risk factors for heavy bleeding.

NCT06765473Not yet recruiting· Phase 3
Misoprostol before or after C-section to prevent bleeding

This study compares two ways of using misoprostol (a medicine that helps the uterus contract) to prevent heavy bleeding after a C-section. One group gets a vaginal tablet before the surgery, the other gets a tablet under the tongue after the surgery.

NCT07188207Not yet recruiting
Rectal misoprostol to reduce blood loss during planned cesarean

This trial tests if giving a medication called misoprostol as a rectal suppository can help reduce bleeding during a planned cesarean section. If you are having a planned cesarean and are generally healthy, this study might be an option for you.

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.