The Use of D5LR Versus LR for Induction of Labor and Time to Delivery in Multiparous and Primiparous Patient's With Favorable and Unfavorable Bishop's Scores

Completed · Not applicable

Conditions studied: Induction of Labor Affected Fetus / Newborn

In brief

Currently, the optimum IV fluid for induction of labor is unknown. The goal of this study is to determine the optimum fluid for induction of labor, D5LR versus LR. The investigators hypothesize that patients assigned to the D5LR group will have a shorter induction of labor when compared to patient's in the LR group.

Key facts

Study ID

NCT03822052

Run by

Ascension Health

People needed

39

Starts

2019-03-15

Expected to finish

2019-12-19

Last updated by the study team

2019-12-23

Who can join

Age: 18 and older, up to 45. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Pregnant women, age 18 - 45, that were admitted for induction of labor without any co-morbid conditions and their respective newborns with
• Induction of labor
• Singleton pregnancies
• Vertex presentation
• Pregnancies at 39 0/7 weeks gestation - 41 6/7 weeks gestation
• All races/ethnicities

You may not qualify if…

• Multifetal gestations
• Noncephalic presentation
• Preexisting medical conditions:
• Maternal cardiac disease
• Lung diseases
• Chronic hypertension
• Pregestational or gestational diabetes
• gHTN or Pre-Eclampsia
• medical indication for induction of labor (olighydramnios, IUGR)

Where it is running

• Ascension Genesys Hospital — Grand Blanc, Michigan, United States

Full record on ClinicalTrials.gov

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