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临床试验/TCTR20140716001
TCTR20140716001招募中4 期

Postoperative pain relief and incidence of chronic pain in patients undergoing arthroscopic shoulder surgery: comparison between interscalene brachial plexus block and parecoxib plus interscalene brachial plexus block

Prince of Songkla University0 个研究点目标入组 86 人开始时间: 2014年7月16日最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
入组人数
86

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 65 Years(—)
性别
All

入选标准

  • Eligible patients are those aged 18 65 years of either sex American Society of Anesthesiologists ASA physical status I II and body mass index BMI between 16 35

排除标准

  • The exclusion criteria are patients who are allergic to sulfonamides or celecoxib with impaired hepatic or renal functions alcohol or substance abuse chronic pain except pain in the shoulder or daily intake of analgesics uncontrolled medical disease hypertension and diabetes mellitus and inability to communicate

研究者

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