临床试验/NCT02163980

NCT02163980已完成不适用

Effect of Dexmedetomidine on the Characteristics of High Volume/Low Concentration Ropivacaine in a Caudal Block in Pediatrics

Yonsei University1 个研究点分布在 1 个国家目标入组 80 人开始时间: 2011年5月最近更新: 2014年6月16日

适应症

干预措施

试验速览

阶段: 不适用
状态: 已完成
发起方: Yonsei University
入组人数: 80
试验地点: 1
主要终点: vital sign

研究概览研究设计入排标准研究组 & 干预措施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 investigators perform this study to evaluate the effects of caudal Dexmedetomidine (DEX) added to high volume/low-concentration of ropivacaine in children undergoing orchiopexy.

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: Triple (Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围: 1 Year 至 6 Years（Child）
性别: Male
接受健康志愿者: 是

入选标准

•children undergoing ambulatory orchiopexy,
•ASA status I

排除标准

•mental retardation,
•developmental delay,
•neurological or psychiatric illness,
•coagulation disorder,
•spinal anomalies

研究组 & 干预措施

Caudal ropivacaine + normal saline

Placebo Comparator

1.5ml kg-1 ropivacaine 0.15% with normal saline (Control group, n=40).

干预措施: Caudal ropivacaine + normal saline (Drug)

Caudal ropivacaine + dexmedetomidine

Experimental

1.5ml kg-1 ropivacaine 0.15% with dexmedetomidine 1 μg kg-1 (DEX group, n=40)

干预措施: Caudal ropivacaine + dexmedetomidine (Drug)

结局指标

主要结局

vital sign

时间窗: up to 180 min after surgery

systolic arterial pressure

次要结局

inhalation anesthetics requirements(up to 180 min after surgery)

研究者

发起方

Yonsei University

申办方类型

Other

责任方

Sponsor

研究点 (1)

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