drugset / Trial / NCT06550089
High Or Low Dose pOstpartUm Oxytocin at the Time of Cesarean Birth
RandomizedParallel-groupOpen-labelPrevention
Summary
This is a study to investigate whether it is feasible to conduct a randomized controlled trial (RCT) of a high dose of oxytocin versus the standard low-dose oxytocin. Further the investigators, aim to assess whether there are differences in health outcomes between both arms of the study.
Timeline
- Start
- 2024-10
- Primary completion
- 2026-10
- Completion
- 2026-12
Outcome
Outcome not reported
Stopped: “Study will be restarted at a later date”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Oxytocin | Peptide | 18 iu | Intravenous |
| Subject | Oxytocin | Peptide | 36 iu | Intravenous |
| Subject | Oxytocin | Peptide | 54 iu | Intravenous |