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Prophylactic Regimen of Intravenous Oxytocin, Intravenous Tranexamic Acid, and Intramuscular Ergot Derivative for Primary Prevention of Postpartum Hemorrhage in Intrapartum Cesarean Section Versus Intravenous Carbetocin Alone
Plain-language guide to NCT07318467: not phased randomized trial of Oxytocin and Carbetocin, 80 participants. Who took part, design and what was measured.
Key Facts
- Registry ID
- NCT07318467
- Phase
- not phased
- Status
- not yet recruiting
- Start
- 2026-01-01
- Completion (planned or actual)
- 2026-06-30
- Participants
- 80 (estimated)
- Design
- randomized, double-blind, prevention
- Conditions studied
- Post Partum Hemorrhage
- Results posted
- not yet
What This Study Did, in Plain Language
What Was Tested
In this not phased trial, researchers set out to test Oxytocin and Carbetocin.
It had two arms (groups): Group A (experimental) and Group B (active comparator).
The registry classes the interventions as drug.
Who Took Part
80 planned participants were the target.
It was open to women only aged from 18 years up to 45 years.
Healthy volunteers could join, not only people with the condition.
Examples of who could join: Women undergoing C-Sections. Women between the ages of 18 and 45 years. Gestational age is equal to or more than 36 weeks. No known coagulopathy or bleeding disorders. No known hypersensitivity or allergy to drugs used in the study.
The full record lists 7 inclusion and 8 exclusion criteria; among the exclusions: hemodynamically unstable or immobile patients; multifetal pregnancy; patients who are receiving prophylactic or therapeutic anticoagulation.
How the Study Was Run
The set-up was randomized, parallel-group and double-blind.
Because people in this Oxytocin study were split into groups at random, differences between the groups are less likely to reflect who happened to join each one.
Groups ran in parallel: each of the participants stayed in one arm throughout.
Neither the participants nor the staff measuring them knew who was on Oxytocin, so expectations could not easily colour the readings.
Those kept unaware of assignments: participant and investigator.
It started in 2026-01-01 with completion listed for 2026-06-30.
Its stated primary purpose is prevention.
What Was Measured
Primary outcome: Amount of blood loss (time frame: during and up to 24 hours after cesarean section).
What This Means in Plain Language
Put simply, this is a not phased, randomized trial of Oxytocin and Carbetocin in 80 people.
Its status is not yet recruiting; no results are posted to the registry yet, so nothing here describes outcomes.
More context: the Oxytocin compound page and the Carbetocin compound page, all human trials.
Our Notes on the Compounds
Oxytocin: A peptide hormone with established obstetric medical uses and a less settled role in research on behavior, sexual function and appetite.
Carbetocin: A long-acting oxytocin analog used outside the US to prevent bleeding after childbirth; also studied intranasally in Prader-Willi syndrome.
Related Pages
Source: ClinicalTrials.gov record. This explanation is written by PeptideWhiz from the public record. For research and education only. Not medical advice; no dosing information is given.