临床试验/NCT00199784

NCT00199784已完成4 期

Hemodynamic Measurements During Cesarean Section With Spinal Anesthesia

Oslo University Hospital2 个研究点分布在 1 个国家目标入组 80 人开始时间: 2005年6月1日最近更新: 2011年7月6日

适应症

试验速览

阶段: 4 期
状态: 已完成
发起方
入组人数: 80
试验地点: 2
主要终点: Differences in cardiac output

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

The purpose of this study is to determine the effect of low dose versus standard dose spinal anesthesia with and without intravenous phenylephrine-infusion on blood pressure, cardiac output and systemic vascular resistance.

详细描述

Hypotension during cesarean section with spinal anesthesia is common. We compare low dose versus standard dose spinal anesthesia with and without intravenous phenylephrine-infusion.

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: Double

入排标准

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

入选标准

•Healthy pregnant women for elective cesarean section

排除标准

•Shorter than 160 or taller than 180 cm
•Pre-pregnant body mass index (BMI) over 32

结局指标

主要结局

Differences in cardiac output

Blood pressure

Systemic vascular resistance

次要结局

Nausea
Fatigue
Cardiovascular instability due to overdosing spinal anesthesia for cesarean section (CS)

研究者

发起方

Oslo University Hospital

申办方类型

Other

研究点 (2)

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