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临床试验/NCT05674838
NCT05674838已完成不适用

Evaluation of the Use of Leg Elevation on a Peanut Ball to Prevent Hypotension Following Epidural Anesthesia in Laboring Women

TriHealth Inc.2 个研究点 分布在 1 个国家目标入组 102 人开始时间: 2022年10月29日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
102
试验地点
2
主要终点
Number of Patients With Maternal Hypotension Requiring Treatment

研究概览

简要总结

When hypotension is related to epidural placement, this can occur within 15-60 minutes after placement. The purpose of this study is to build upon this preliminary work and to use a randomized controlled trial to examine the effectiveness of leg elevation in preventing hypotension among a larger sample of laboring women who receive an epidural analgesia. This study will use a randomized, non-blinded, controlled design with two arms:

Arm 1: Patient will be put in a left tilt position with her hip on a wedge and both legs elevated on a peanut ball. She'll remain in this position for approximately 40 minutes.

Arm 2: Patient will be put in a left tilt position with her hip on a wedge and no leg elevation. She'll remain in this position for approximately 40 minutes.

详细描述

When hypotension is related to epidural placement, this can occur within 15-60 minutes after placement. The purpose of this study is to build upon this preliminary work and to use a randomized controlled trial to examine the effectiveness of leg elevation in preventing hypotension among a larger sample of laboring women who receive an epidural analgesia. This study will use a randomized, non-blinded, controlled design with two arms:

Arm 1: Patient will be put in a left tilt position with her hip on a wedge and both legs elevated on a peanut ball. She'll remain in this position for approximately 40 minutes.

Arm 2: Patient will be put in a left tilt position with her hip on a wedge and no leg elevation. She'll remain in this position for approximately 40 minutes.

Outcome variables include occurrence of maternal hypotension or late or prolonged decelerations within the first hour after epidural placement.

研究设计

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

入排标准

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

入选标准

  • Laboring at Good Samaritan Hospital Labor & Delivery Unit
  • 37+ weeks gestation
  • Planned vaginal delivery
  • Planned epidural analgesia

排除标准

  • Under 18 years old
  • Does not speak English
  • Unable to consent to involvement in the research study
  • Attended less than 3 prenatal care office visits
  • Diagnosed with fetal demise
  • Diagnosed with fetal anomalies
  • Contraindications to both legs being elevated (ex: fractured bones, lower limb amputation, etc.)
  • Contraindications to receiving 1L of IV fluids
  • Requiring IV hypertensive medications
  • Requiring IV magnesium

结局指标

主要结局

Number of Patients With Maternal Hypotension Requiring Treatment

时间窗: 40 minutes

SBP requiring treatment by the anesthesia provider

Number of Patients With Late or Prolonged Decelerations on the Fetal Heart Tracings

时间窗: 40 minutes

Any late or prolonged decelerations on the fetal heart tracings

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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