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Nipple Stimulation for Labor Induction: Efficiency, Safety and Satisfaction Measures (NCT03025503)

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
    Ages eligible for Study
    18 Years to 45 Years
    Genders eligible for Study
    Female
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Inclusion Criteria:
    • 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%.
    Exclusion Criteria:
    • Water break > 24 hours at the time of admission to the delivery room
    • Active vaginal bleeding with suspected placental abruption
    • Maternal fever
    • Multifetal pregnancy
    • Women with contraindication for vaginal birth
    • Preeclampsia
    • IUGR (intrauterine growth restriction)
    • Macrosomia
    • Non-reassuring fetal heart tracing

    1 locations

    Israel (1)
    • Hadassah Medical Organization, Jerusalem, Israel
      Not specified
      Jerusalem, Israel
    Status:
    not yet recruiting
    Type:
    Interventional
    Phase:
    -
    Start:
    31 December, 2016
    Updated:
    15 January, 2017
    Participants:
    100
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