Clinical Trials Directory

Trials / Terminated

TerminatedNCT03246919

Ideal Time of Oxytocin Infusion During Cesarean Section

Status
Terminated
Phase
Phase 4
Study type
Interventional
Enrollment
68 (actual)
Sponsor
Loyola University · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Accepted

Summary

This study will evaluate if the timing of oxytocin administration in cesarean deliveries will affect the amount of maternal blood loss. Half of participants will receive oxytocin after delivery of the fetal anterior shoulder and the other half will receive oxytocin after delivery of the placenta. We hypothesize that administering oxytocin after delivery of the shoulder, will result in less overall maternal blood loss.

Detailed description

Oxytocin is a routinely administered medication for both vaginal and cesarean deliveries in the third stage of labor, as part of standard of care in the United States. This medication helps to reduce overall blood loss, by functioning as a uterotonic. Currently evidence is lacking to direct timing of oxytocin administration in cesarean deliveries. This study will evaluate both estimated and quantitative blood loss for both groups of patients. It will also compare the change from pre-operative to post-operative hemoglobin levels.

Conditions

Interventions

TypeNameDescription
DRUGOxytocinOxytocin is administered after delivery of the fetal anterior shoulder, rather than being administered after delivery of the placenta
DRUGPlaceboPlacebo will be administered after delivery of the placenta

Timeline

Start date
2017-09-13
Primary completion
2020-02-24
Completion
2020-02-24
First posted
2017-08-11
Last updated
2020-06-18

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03246919. Inclusion in this directory is not an endorsement.