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Clinical Trial Summary

The purpose of this study is to evaluate the differences in blood clotting seen in healthy patients given two different doses of oxytocin following cesarean delivery. The secondary objectives are to evaluate changes in blood pressure, rates of nausea and vomiting, and differences in blood loss with the two separate doses of oxytocin.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Basic Science


Related Conditions & MeSH terms

  • Coagulation Changes With Oxytocin

NCT number NCT02063568
Study type Interventional
Source Duke University
Contact
Status Withdrawn
Phase N/A
Start date January 2015
Completion date December 2015