Comparing High Versus Low Dose of Oxytocin, in Gravida Women With BMI 30 and Above Which Are Undergoing Induction of Labor

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexFemale
AgeNot listed
SponsorHaEmek Medical Center, Israel

About this trial

The goal of this clinical trial is to compare between higher and lower dose of oxytocin to induce delivery in obese women. Researches will compare between low and high doses of oxytocin. the study group will use high dose of oxytocin (20 units in 1000 ml) versus the control group which will use low dose of oxytocin (10 units of oxytocin in 1000 ml)

Eligibility criteria

Qualifiers

Women at term (37-42 weeks), requiring the use of oxytocin for induction of labor or for augmentation of labor.

BMI 30 and above

Viable singleton pregnancies

Cephalic presentation.

Disqualifiers

Women with previous cesarean delivery

Multiple pregnancy

Multiple fetal malformations

IUFD

Trial design

Treatments tested in this trial

  • Oxytocin Grindeks 10 IU/ml- solution for injection

Treatment groups

130 Participants
are divided into 2 treatment groups

Sponsors and collaborators