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Clinical Trials in Israel / NCT06990217
Starting soon Phase 4

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

NCT06990217 · tracked via the Priya Life Science Israel tracker
Phase
Phase 4
Started
2025-06
Last updated
2025-05-25

Condition(s) studied

Induction of LaborAugmentation of Labor

Investigational drug(s) / intervention(s)

Oxytocin Grindeks 10 IU/ml- solution for injection →

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)

Trial sites (1)

FacilityCityRegionStatus
Haemek Medical Center Afula Israel

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Official registry record

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.

View NCT06990217 on ClinicalTrials.gov ↗ ← All trials in Israel