Status:

UNKNOWN

Balloon Catheter Combined With Oxytocin Induction Among the Pregnant Women With Previous Cesarean Section

Lead Sponsor:

The First Affiliated Hospital with Nanjing Medical University

Conditions:

Trial of Labor After Cesarean

Vaginal Birth After Cesarean

Eligibility:

FEMALE

20-40 years

Brief Summary

This study is a multi-center, prospective, observational clinical trial study. 924 full-term pregnant women will be enrolled as subjects, and the ratio of eligible subjects in the two groups is 1:1. I...

Eligibility Criteria

Inclusion

  • Inclusion Criteria:
  • Volunteers sign the informed consent;
  • Age: 20-40 years;
  • Singleton, a cephalic presentation;
  • No contradiction to vaginal delivery; 5.39\~42 weeks.
  • Exclusion criteria:
  • Konwn contraindication to vaginal delivery or severe complications;
  • Multiple gestation;
  • Uterine malformation;
  • Severe psychiatric disorder;
  • Without family's support.

Exclusion

    Key Trial Info

    Start Date :

    January 30 2022

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ESTIMATED

    End Date :

    December 30 2024

    Estimated Enrollment :

    924 Patients enrolled

    Trial Details

    Trial ID

    NCT05246761

    Start Date

    January 30 2022

    End Date

    December 30 2024

    Last Update

    April 22 2022

    Active Locations (1)

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    1

    First Affiliated Hospital of Nanjing Medical University

    Nanjing, Jiangsu, China

    Balloon Catheter Combined With Oxytocin Induction Among the Pregnant Women With Previous Cesarean Section | DecenTrialz