Clinical Trials Directory

Trials / Completed

CompletedNCT03344302

Oxytocin Administration During Cesarean Section

Oxytocin Administration During Cesarean Section Before Versus After Fetal Delivery Randomized Clinical Trial

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
200 (actual)
Sponsor
Assiut University · Academic / Other
Sex
Female
Age
20 Years – 40 Years
Healthy volunteers
Not accepted

Summary

Cesarean delivery is defined as fetal birth through incisions in the abdominal wall and the uterine wall. This definition does not include removal of the fetus from the abdominal cavity in the case of uterine rupture or in the case of an abdominal pregnancy The guidelines of the Royal College of Obstetricians and Gynaecologists on caesarean section recommend a slow intravenous bolus dose of 5 IU of oxytocin after delivery of the infant. Intravenous oxytocin has a short half life (4-10 minutes); therefore the potential advantage of an oxytocin infusion at caesarean section is in maintaining uterine contractility throughout the surgical procedure and immediate postpartum period, when most primary haemorrhage occurs

Conditions

Interventions

TypeNameDescription
DRUGOxytocinintravenous infusion of oxytocin 30 units over 5 minutes diluted into 500 mL of normal 0.9% sodium chloride

Timeline

Start date
2016-10-01
Primary completion
2017-08-01
Completion
2017-09-01
First posted
2017-11-17
Last updated
2018-04-23

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT03344302. Inclusion in this directory is not an endorsement.