Have you or your loved ones been diagnosed with failed induction of labor?

You may be eligible to participate in a failed induction of labor clinical trial.

Have you or your loved ones been diagnosed with failed induction of labor? You may be eligible to participate in a failed induction of labor clinical trial.

What is a clinical trial? Is participating in a clinical trial right for you? Learn more

Failed Induction of Labor Clinical Trial in Seongnam-si Gyeonggi-do

NCT02618096 | Interventional

Have you or your loved ones been diagnosed with failed induction of labor?

You may be eligible to participate in a failed induction of labor clinical trial.

Have you or your loved ones been diagnosed with failed induction of labor? You may be eligible to participate in a failed induction of labor clinical trial.

Completed

Female

All ages

This study has recruited 154 Participants

The purpose of this study is to compare concurrent oxytocin with membrane sweeping versus dinoprostone pessary in labor induction for multiparas at term with an unfavorable cervix.

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Details for the study

Brief Title

Concurrent Oxytocin With Membrane Sweeping Versus Dinoprostone Pessary in Labor Induction of Multiparous Women at Term

Official Title

Brief Summary

The purpose of this study is to compare concurrent oxytocin with membrane sweeping versus<br /> dinoprostone pessary in labor induction for multiparas at term with an unfavorable cervix.

Outcome Measures

Outcome measures are the tests that investigators perform to prove whether or not a treatment being tested in a clinical trial is having any effect.

Primary

Vaginal delivery within 24 hours

Vaginal delivery within 24 hours is defined as vaginal delivery after 24 hours of initiating intervention (i.e. membrane sweeping or dinoprostone) on the first day of induction.

From the time of initiating intervention (i.e. membrane sweeping or dinoprostone) until the time of vaginal delivery, assessed up to 24 hours

Secondary

Successful labor induction

to achieve the active phase of labor corresponding to a cervical dilatation of >=4cm

From the time of initiating intervention (i.e. membrane sweeping or dinoprostone) until the time of active phase of labor (defined as a cervical dilatation of >=4cm), assessed up to 24 hours

Study Criteria

Inclusion Criteria:

  -  singleton pregnancy

  -  Multiparous women

  -  gestational age >=37.0 weeks

  -  Bishop score <=6

  -  intact amniotic membrane

  -  absence of labor

  -  live fetus with vertex presentation

  -  no previous uterine surgical procedure

Exclusion Criteria:

  -  Multiple pregnancy

  -  Placenta previa