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临床试验/NCT03065569
NCT03065569已完成不适用

A Comparison of Epidural Techniques for Labour Analgesia

University of British Columbia2 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2017年5月7日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
150
试验地点
2
主要终点
Bupivacaine requirement for analgesia

研究概览

简要总结

A trial comparing outcomes for different epidural techniques in labour analgesia

详细描述

Epidurals are the most common form of pain relief in labour. There are two techniques in use at the moment to place the epidural: epidural or combined spinal epidural (CSE). CSE has been shown to work faster and provide better pain relief than epidural alone. The investigators aim to show that CSE also requires less medication over the course of labour as this may mean it has fewer side effects. The amount of medication needed during labour between the two different techniques given in a standardized way will be compared.

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
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Healthy, singleton presentation at term

排除标准

  • Significant comorbidities likely to alter outcome of labour

研究组 & 干预措施

Standard Epidural Technique

Active Comparator

Epidural will be performed Initial dose of 16 mL of 0.125% bupivacaine will be given Upon patient request, rescue bolus based on protocol will be administered.

干预措施: Bupivacaine (Drug)

Combined Spinal Epidural Technique

Experimental

CSE will be performed Initial dose of 16 mL of 0.125% bupivacaine will be given Upon patient request, rescue bolus based on protocol will be administered.

干预措施: Bupivacaine (Drug)

结局指标

主要结局

Bupivacaine requirement for analgesia

时间窗: From randomization until delivery

milligram of bupivacaine used per hour

次要结局

未报告次要终点

研究者

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

Anton Chau

Clinical Assistant Professor

University of British Columbia

研究点 (2)

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