Phase
Condition
N/ATreatment
Induction of labor
Clinical Study ID
Ages 18-60 Female Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Women above 18 years old
Sign an informed consent
Term pregnancy (>37 weeks)
Viable fetus
Singleton
Vertex presentation
Intact membranes
Cervix with Bishop score ≤6
Exclusion
Exclusion Criteria:
Previous cesarean delivery
Major fetal malformations
Contraindication to spontaneous vaginal delivery
Amniotic fluid index >25cm
Chorioamnionitis at admission
Placental abruption
Previous prostaglandin use for induction of labor
A low-lying placenta (up to 2 cm from the internal os)
Carriers of hepatitis B or C or human immunodeficiency viruses,
Women with a history of allergy to latex.
Women with a history of allergy to castor oil
Study Design
Study Description
Connect with a study center
Holy Family hospital, Nazareth
Nazareth,
IsraelActive - Recruiting
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