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Clinical Implications of Fetal Positioning During Delivery

2021年4月29日 更新者:Barbara Baranowska、Żelazna Medical Centre, LLC
The project aims to find a relationship between the positioning of the foetus before and during birth and the results of obstetrics and to determine their incidence in the Polish population. The study will be conducted by combining the use of ultrasound diagnostics, midwives observations during childbirth, analysis of medical documentation and a questionnaire on the activity of examined women. The obtained results will be used to prepare guidelines for the birth in a particular foetus position.

研究概览

地位

招聘中

干预/治疗

详细说明

The purpose of the examination is to describe the difficulties associated with delivery in a non-optimal position of the fetus. Initial observations show that such childbirth is perceived as difficult by both the women giving birth and the staff. The aim of the study is to describe the level of difficulty of this labor, expressed as the experience of the woman, as well as all the elements that may affect the difficulty of this labor, for example, slower or no progress in labor, disturbances in systolic function, injuries, the need to use epidural anesthesia, increased blood loss.

研究类型

观察性的

注册 (预期的)

300

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

    • Mazowieckie
      • Warsaw、Mazowieckie、波兰、01-004
        • 招聘中
        • Żelazna Medical Centre, LLC
        • 接触:

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

女性

取样方法

非概率样本

研究人群

women coming to the 3rd level hospital with a birth house. During a physiological pregnancy, with no severe coexisting diseases.

描述

Inclusion Criteria:

  • during childbirth,
  • in a single pregnancy,

Exclusion Criteria:

  • pelvic position of the fetus
  • in whom labor is induced for reasons other than post-term pregnancy,
  • women who came to the hospital in the second stage of labor
  • severe diseases mother or foetus.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Mode of delivery
大体时间:immediately after delivery
Mode of delivery as measured by number of women who had a vaginal, instrumental or operational delivery.
immediately after delivery

次要结果测量

结果测量
措施说明
大体时间
Duration of delivery
大体时间:immediately after birth
the time of 1,2,3 and 4 stage of labor
immediately after birth
Uterine contractions
大体时间:during birth
uterine contractions as measured by number of contractions and assessment of uterine contractile coordination
during birth
Labor progress
大体时间:during birth
Labor progress as measured by assessment of the head insertion, advancement in the birth canal,
during birth
Epidural
大体时间:immediately after delivery
as measured by epidural or not
immediately after delivery
Perineum injury
大体时间:immediately after delivery
as measured by number and extent of injury
immediately after delivery
Episiotomy
大体时间:immediately after delivery
as measured by episiotomy or not
immediately after delivery
Methods of placental separation
大体时间:immediately after delivery
as measured by number of Duncan or SchultZ methods
immediately after delivery
Blood loss
大体时间:immediately after delivery
postpartum blood loss (ml)
immediately after delivery
Difficulty of childbirth
大体时间:immediately after delivery
difficulty of childbirth as measured by subjective assessment of the woman and the midwife
immediately after delivery

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 学习椅:Baranowska Baranowska, PhD、Żelazna Medical Centre, LLC

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2021年3月31日

初级完成 (预期的)

2021年6月30日

研究完成 (预期的)

2021年12月30日

研究注册日期

首次提交

2021年3月12日

首先提交符合 QC 标准的

2021年3月19日

首次发布 (实际的)

2021年3月24日

研究记录更新

最后更新发布 (实际的)

2021年4月30日

上次提交的符合 QC 标准的更新

2021年4月29日

最后验证

2021年4月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • PN/29/2020

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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