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Clinical Trial Summary

Introduction: postpartum hemorrage is a leading cause of death after cesarean sections in Brazil. Oxytocin is the main drug for both prophylaxis and threatment of postpartum hemorrage because uterine atony is the most prevalent cause. Both excessive and too low oxytocin doses threaten the life of women.

Objective: to determine the minimum effective dose of oxytocin for cesareans during labor.

Method: adaptative clinical trial using a modified up and down method of two sequential groups: rule of three and continuous infusion. Allocation in rule of three or continuous infusion will be random and masked for patients and anesthesiologists. The minimum effective dose will be the effective dose for 90% of success (ED90 for preventing uterine atony).


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT02794779
Study type Interventional
Source Brasilia University Hospital
Contact Gabriel MN Guimaraes, MD, MSc
Phone +5561996455997
Email gabrielmng@gmail.com
Status Recruiting
Phase Phase 3
Start date July 2016
Completion date December 2017