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临床试验/NCT07549971
NCT07549971已完成不适用

Trial of Labor After Cesarean

G. d'Annunzio University0 个研究点目标入组 1,200 人开始时间: 2015年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
1,200
主要终点
incidence of maternal request for trial of labor

研究概览

简要总结

in 2015 a protocol for trail of labor after a single cesarean delivery was approved by medical committee of Pescara Hospital. A database from outpatient clinic evaluated all women after 34 weeks' gestation with a previous cesarean delivery. Patients with a specific medical indication for cesarean delivery were skipped, whilst the others were recruited within repetitive elective cesarean delivery or trial of labor based on maternal request. Patients were couselled on the opportunity of having a mechanical induction/ rupture of membranes and subsequent oxytocin infusion if needed due to prolonged gestation (above 41 weeks plus 3 days) or medical indication to delivery (i.e. gestational diabetes, hypertension, SGA, etc.)

详细描述

All pregnant women with a previous CD attending Labor Ward of Santo Spirito Hospital of Pescara Italy (affiliated to University of Chieti Pescara) were enrolled at outpatient clinic after internal protocol registration for trial of labor in previus cesarean delivery. Patinets with a medical indication to CD were not elegible. Sociodemographic data such as ethnic background, maternal age, gestational age at delivery, previous vaginal birth, indications to previous CD, and maternal willingness to RECD ot TOLAC were recorded.

Maternal decision to switch to different intervention were recorded. Outcome of RECD and TOLAC were recorded.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 57 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • pregnant women
  • previous CD

排除标准

  • below 34 weeks' gestation
  • medical indication to CD

结局指标

主要结局

incidence of maternal request for trial of labor

时间窗: 11 years

incidence of women with request of trial of labor through the time

incidence of VBAC

时间窗: 11 years

number of vaginal birth through the time

次要结局

  • maternal adverse outcome(11 years)
  • neonatal adverse outcome(11 years)

研究者

发起方
G. d'Annunzio University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Claudio Celentano

MD

G. d'Annunzio University

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