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临床试验/NCT02544893
NCT02544893已完成4 期

Postoperative Analgesic Effects of Using Bupivacaine Alone or Added Dexmedetomidine for Ultrasound Guided Thoracic Paravertebral Block in Thoracotomy

TC Erciyes University1 个研究点 分布在 1 个国家目标入组 93 人开始时间: 2015年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
93
试验地点
1
主要终点
opioid consumption

研究概览

简要总结

we aimed postoperative analgesic effects of using bupivacaine alone or added dexmedetomidine for ultrasound guided thoracic paravertebral block in thoracotomy

详细描述

paravertebral block is commonly used in the treatment for acute and chronic pain.The duration of paravertebral block could theoretically be prolonged with neurolytic agents. Dexmedetomidine ,an alfa-2 adrenoreceptor agonist, is being used and adjuvant capable of prolonging duration of sensory and motor block on nerve blocks.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 18-65 aged
  • patient undergoing thoracotomy

排除标准

  • chronic opioid consumption
  • bupivacaine and dexmedetomidine allergies
  • coagulopathy
  • infection at the needle insertion side
  • chronic liver and kidney disease

研究组 & 干预措施

bupivacaine

Active Comparator

0,5% 20 ml bupivacaine added 0.9% 1 ml serum physiologic on paravertebral block

干预措施: bupivacaine (Drug)

dexmedetomidine

Active Comparator

100 mcg dexmedetomidine added to 0,5% 20 ml bupivacaine on paravertebral block

干预措施: dexmedetomidin (Drug)

serum phsyologic

Active Comparator

0,9% 21 ml serum physiologic

干预措施: serum physiologic (Drug)

结局指标

主要结局

opioid consumption

时间窗: postoperative 24 hours

patient controlled analgesia

次要结局

  • visual analog scale(postoperative 1 day)

研究者

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

Esra Nur Ünalan

resident

TC Erciyes University

研究点 (1)

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