Pharmacokinetics of Oxytocin at Cesarean Delivery

Completed

Conditions studied: Postpartum Hemorrhage

In brief

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.

Key facts

Study ID

NCT03898882

Run by

Washington University School of Medicine

People needed

30

Starts

2019-05-24

Expected to finish

2020-02-28

Last updated by the study team

2020-05-07

Who can join

Age: 18 and older, up to 45. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Term singleton pregnancy
• Age 18-45 years of age
• ASA classification 2 or 3
• Scheduled cesarean delivery under neuraxial anaesthesia

You may not qualify if…

• Age or ASA classification outside of inclusion criteria
• Need for general anaesthesia
• Absence of consent
• Inability to communicate in English or other barrier to providing informed consent

Where it is running

• Washington University in St. Louis — St Louis, Missouri, United States

Full record on ClinicalTrials.gov

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