跳至主要内容
临床试验/NCT00711451
NCT00711451终止不适用

Manual and Expressed Placental Removal at Planned Cesarean Delivery and Its Effects on Various Cardiac Indices as Measured By Continuous Wave Doppler Ultrasonography

Corewell Health East2 个研究点 分布在 1 个国家目标入组 19 人开始时间: 2008年7月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
19
试验地点
2
主要终点
Hemodynamic profile, especially Systemic Vascular Resistance

研究概览

简要总结

The purpose of this study is to evaluate whether manual removal of the placenta during a cesarean delivery results in higher changes in the resistance of blood flow throughout the body, also called systemic vascular resistance (SVR)

详细描述

Patients presenting to William Beaumont Hospital Royal Oak Labor and Delivery for a scheduled low transverse cesarean delivery will be asked to participate in a prospective, randomized study to evaluate any changes in systemic vascular resistance (SVR) pre- and post-delivery.

After obtaining informed consent, the patients will be randomized to one of two groups: group 1 will have manual removal of the placenta at cesarean section and group 2 will have expressed removal of the placenta at cesarean section.

Both groups will have a pre-operative continuous wave Doppler evaluation and a post-operative continuous wave Doppler evaluation at 24 hours after delivery. Continuous wave Doppler evaluation will be used pre- and post-operatively to evaluate any changes in SVR.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • scheduled for cesarean delivery
  • able to give informed consent

排除标准

  • taking medications that may affect hemodynamics
  • unable to give informed consent

研究组 & 干预措施

manual

Active Comparator

Manual removal of placenta

干预措施: Manual removal (Behavioral)

expressed

Active Comparator

expressed placental removal

干预措施: Expressed removal (Procedure)

结局指标

主要结局

Hemodynamic profile, especially Systemic Vascular Resistance

时间窗: immediately before and 24 hours after cesarean delivery

次要结局

  • development of postpartum preeclampsia(within 1 week of delivery)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

John Uckele

Attending Physician

Corewell Health East

研究点 (2)

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