跳至主要内容
临床试验/KCT0005197
KCT0005197已完成未知

Programmed intermittent bolus infusion versus continuous infusion of 0.2% ropivacaine after ultrasound-guided continuous interscalene brachial plexus block in arthroscopic shoulder surgery

Pusan National University Yangsan Hospital0 个研究点目标入组 64 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
64

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
19?(Year) 至 0No Limit(—)
性别
All

入选标准

  • American Society of Anesthesiology physical status I-III patients scheduled for arthroscopic shoulder surgery

排除标准

  • Patients who lack the ability to understand or perform the test in this study, patients with deficiency of blood clotting, patients with brachial plexus lesions, those with neurological defects at the treatment site, allergic reactions to ropivacaine in previous surgery or procedures, and pregnant women are excluded.

研究者

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