Oxytocin Grindeks 10 IU/ml- solution for injection: our study is aims to compare two oxytocin regimens - low VS high dose among obese women who need induction or augmentation of labor
Study summary
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
Sex
FEMALE
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* 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.
* No contraindication for vaginal delivery
Exclusion Criteria:
* Women with previous cesarean delivery
* Multiple pregnancy
* Multiple fetal malformations
* IUFD
Primary outcome measure(s)
Time from the start of oxytocin to delivery — from the start of induction till delivery our hypothesis that high dose of oxytocin shortens the time from the start of induction to delivery
Trial sites (1)
Facility
City
Region
Status
Haemek Medical Center
Afula
Israel
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This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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