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Effects of Oxytocin on Bleeding Outcomes During Dilation and Evacuation

Hemorrhage Clinical Trial

Official title:
A Randomized Double-blinded Controlled Trial Comparing Dilation and Evacuation Outcomes With and Without Oxytocin Use

Clinical Trial Summary

Currently, there is very little research to identify ways to decrease blood loss during D&E (dilation and evacuation) procedures. The objective is to determine whether routine use of intravenous oxytocin will improve bleeding outcomes at the time of D&E at 18-24-weeks gestation. To evaluate the hypothesis, investigators will perform a randomized, double-blinded, placebo-controlled trial. The patient will be followed until discharged from the postoperative care unit during which time patient satisfaction, pain score and postoperative bleeding will be assessed.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02083809
Study type Interventional
Source University of Hawaii
Contact
Status Completed
Phase N/A
Start date October 2014
Completion date February 2018
View Details
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