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Pharmacokinetics of Oxytocin at Cesarean Delivery — Peacocks  

Postpartum Hemorrhage Clinical Trial

Official title:
The Pharmacokinetics of Oxytocin in Pregnant Women Undergoing Cesarean Delivery - a Feasibility Pilot Study

Clinical Trial Summary

The primary objective is to obtain data to inform the design of a population pharmacokinetic study of oxytocin after administration at CD as per standard institutional practice.

Clinical Trial Description

In this pilot study the investigators will compare plasma oxytocin concentrations measured in arterial and venous blood, after oxytocin administration at cesarean delivery, in order to assess the validity of venous samples. They will also measure oxytocinase to explore how levels vary around the time of delivery of the placenta and to assess the effect that this may have on the metabolism of oxytocin. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03898882
Study type Observational
Source Washington University School of Medicine
Contact
Status Completed
Phase
Start date May 24, 2019
Completion date February 28, 2020
View Details
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