This study will examine the use of nipple stimulation for cervical ripening in women who
present to the labor and delivery ward after their water has broken but have a
contraindication to prostaglandins.
Other: nipple stimulation
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Full eligibility criteria for NCT03025503
Ages eligible for Study
18 Years to 45 Years
Genders eligible for Study
Accepts Healthy Volunteers
Week 37 + 0 and on
PROM (premature rupture of membranes)
Multiparity (birth sixth or higher) or TOLAC (trial of labor after Caesarean section)
Not in active labor - without regular contractions fetal monitor, cervical dilation < 4 cm and effacement < 80%.
Water break > 24 hours at the time of admission to the delivery room
Active vaginal bleeding with suspected placental abruption
Women with contraindication for vaginal birth
IUGR (intrauterine growth restriction)
Non-reassuring fetal heart tracing
All locations for NCT03025503
Hadassah Medical Organization, Jerusalem, Israel
View full eligibility
Tris trial is registered with FDA with number: NCT03025503. The sponsor of the trial is Hadassah Medical Organization and it is looking for 100 volunteers for the current phase.
Official trial title: Nipple Stimulation for Labor Induction: Efficiency, Safety and Satisfaction Measures
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