临床试验/CTRI/2018/03/012750

CTRI/2018/03/012750已完成4 期

To compare 0.5% ropivacaine and 0.5% bupivacaine in supraclavicular brachial plexus block in upper limb surgery.

Department of Anaesthesia0 个研究点目标入组 60 人开始时间: 待定最近更新: 2021年11月24日

试验速览

阶段: 4 期
状态: 已完成
发起方: Department of Anaesthesia
入组人数: 60

研究概览入排标准研究者记录与标识符相似试验

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

入选标准

•60 patients of either sex of ASA class 1 or 2

排除标准

•History of respiratory ,cardiac ,hepatic or renal disease,pregnant women, any history of bleeding disorders,local infection at the site of injection,patient sensitive or allergic to bupivacaine or ropivacaine.

研究者

发起方

Department of Anaesthesia

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