Status:
UNKNOWN
The Effectiveness and Safety of the Trial of Labor in Full Term Pregnant Women With Cesarean Section After Spontaneous Labor
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. 510 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; 6.Spontaneous labor
- 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 28 2022
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
June 30 2025
Estimated Enrollment :
510 Patients enrolled
Trial Details
Trial ID
NCT05215041
Start Date
January 28 2022
End Date
June 30 2025
Last Update
April 25 2022
Active Locations (1)
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1
First Affiliated Hospital of Nanjing Medical University
Nanjing, Jiangsu, China