NCT01828853UnknownNot Applicable
Maternal and Neonatal Outcomes After Membrane Sweeping
Hadassah Medical Organization1 site in 1 country1,200 target enrollmentStarted: April 2013Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Enrollment
- 1,200
- Locations
- 1
- Primary Endpoint
- Neonatal sepsis
Study Overview
Brief Summary
This study aim to estimate maternal and neonatal outcomes after membrane sweeping in different group of patients.
Detailed Description
Sweeping of the membranes is a simple technique usually performed during vaginal examination, in order to initiate labour by increasing local production of prostaglandins.
Study Design
- Study Type
- Observational
- Observational Model
- Case Control
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 17 Years to 45 Years (Child, Adult)
- Sex
- Female
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Women with a singleton pregnancy and confirmed cephalic presentation at or after 37 weeks of gestation who are candidate for vaginal delivery were eligible for the study
Exclusion Criteria
- •Women with a multiple pregnancy, nonreassuring cardiotocogram, meconium stained amniotic fluid, major fetal anomalies, HELLP (hemolysis, elevated liver enzymes, and low platelets) syndrome, or severe preeclampsia and signs of intrauterine infections were not eligible.
- •women who are not candidates for vaginal delivery: placenta previa, breech presentation, planned repeat cesarean.
Outcomes
Primary Outcomes
Neonatal sepsis
Time Frame: Neonates will be followed for the duration of hospital stay, an expected average of 2-3 days
Secondary Outcomes
- Neonatal infection(Neonates will be followed for the duration of hospital stay, an expected average of 2-3 days)
Investigators
Study Sites (1)
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