Feasibility, safety and effectiveness of patient-controlled analgesia using new device with micropump

Shimizu Kazuyoshi0 个研究点目标入组 5 人开始时间: 2019年9月17日最近更新: 2023年10月17日

试验速览

阶段: 未知
状态: 已完成
发起方
入组人数: 5

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

This PCA device with new micropump was clinically used for postoperative pain without any serious complications in 5 patients. Physicians who used this device satisfied with the quality of device.

研究设计

研究类型: Interventional

入排标准

年龄范围: >= 20age old 至 < 80age old（—）
性别: All

入选标准

•Patients who meet all of the following;
•1)Patients who are eligible for PCA using this device intravenously or epidurally after operations under general anesthesia.
•2)Age >= 20 and <80
•3)Patients who undergo surgeries or procedures without public insurance
•4)Patients who are able to obtain own consent by themselves
•5) Patients who will admit to the Intensive Care Unit

排除标准

•Patients who meet at least one of the following;
•1)Severe heart failure (NYHA class 3 or 4)
•2)Severe respiratory failure (Hugh-Jones class 3 or 4)
•3)Past history of psychiatric disease
•4)Past allergic history of local anesthetics and narcotics
•5)Withdraw consent before starting PCA
•6)Pregnant and lactating women
•7) Investigator judged to be inappropriate for this research
•In case of epidural PCA
•8)Severe infection on the insertion site
•9)Severe coagulopathy

研究者

发起方

Shimizu Kazuyoshi

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