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临床试验/NCT02195037
NCT02195037已完成不适用

Changes in Cardiac Output During Delayed Umbilical Cord Clamping

Sharp HealthCare1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2014年7月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
20
试验地点
1
主要终点
Cardiac Output

研究概览

简要总结

Recently, the American College of Obstetricians and Gynecologists (ACOG) recommended a delay of 30-60 seconds in umbilical cord clamping for all newborn infants. This delay allows the newborn to receive his/her own blood from the placenta (placental transfusion) which helps their transition in the first hours of life. The purpose of the study is to learn about the amount of blood flow to and from the baby's heart during normal newborn transition

研究设计

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

入排标准

年龄范围
— 至 1 Minute(Child)
性别
All
接受健康志愿者

入选标准

  • Healthy full term infants
  • Delivered by vaginal birth
  • Estimated gestational age of 37+0to 41+6 weeks corrected gestational age

排除标准

  • Multiples
  • Known fetal anomalies (including cardiac defects).
  • Instrumentation during delivery (forceps or vacuum)
  • Non-reducible nuchal cord during delivery.
  • Any maternal or neonatal indication requiring immediate cord clamping.

结局指标

主要结局

Cardiac Output

时间窗: 5 minutes of Life

次要结局

  • Hemoglobin level(until discharge)
  • Stroke Volume(5 Minutes of Life)
  • Bilirubin level(until discharge)

研究者

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

Anup Katheria, M.D.

Director of Neonatal Research

Sharp HealthCare

研究点 (1)

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