An Evidence Based Protocol for Oxytocin Administration in Vaginal Delivery

Status Withdrawn

Clinical Trial Summary

The purpose of this study will be to evaluate a standardized, evidence-based protocol versus a conventional approach for the dosing of oxytocin in vaginal delivery.

Clinical Trial Description

A traditional practice in many US hospitals includes use of 10-40 IU of Oxytocin mixed in various volumes of crystalloid administered at an unspecified and uncontrolled rate (quite often off the pump) in order to restore uterine tone and minimize routine blood loss in the third stage of labor. Many practitioners question high dose oxytocin regimens, timing and duration of Oxytocin administration for postpartum hemorrhage prophylaxis. Given the lack of a universally accepted, evidence based protocol, this study aims at comparing the efficacy of a traditional approach of administration of Oxytocin with an evidence-based designed algorithm. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02410655
Study type	Interventional
Source	New York University School of Medicine
Contact
Status	Withdrawn
Phase	Phase 4
Start date	November 2015
Completion date	July 27, 2017

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See also
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