Overview
An Evidence Based Protocol for Oxytocin Administration in Vaginal Delivery
Status:
Withdrawn
Withdrawn
Trial end date:
2017-07-27
2017-07-27
Target enrollment:
0
0
Participant gender:
Female
Female
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.Phase:
Phase 4Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
New York University School of Medicine
NYU Langone HealthTreatments:
Oxytocin
Criteria
Inclusion Criteria:- Vaginal Delivery
Exclusion Criteria:
- Cesarean Delivery
- Allergy to Oxytocin
- Cardiac Arrhythmia