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临床试验/JPRN-UMIN000037225
JPRN-UMIN000037225已完成未知

A prospective randomized controlled trial of the usefulness of the bispectral index (BIS) monitor in propofol sedation with double-balloon endoscopic retrograde cholangiopancreatography (DB-ERCP) for postoperative reconstructed intestinal cases - A prospective randomized controlled trial of the usefulness of the bispectral index (BIS) monitor in propofol sedation with double-balloon endoscopic retrograde cholangiopancreatography (DB-ERCP) for postoperative reconstructed intestinal cases

Okayama University Hospital0 个研究点目标入组 100 人开始时间: 2019年7月1日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
100

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
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1)Patients less than 20 years old 2)Pregnant woman 3)Patients with egg, soy, propofol allergy 4)Patients with hypotension (less than 90/50 mmHg) or bradycardia (less than 50bpm), and patients receiving oxygen prior to sedation 5)Patients with ASA-Performance status 4-6 6)Patients already registered in this study 7)Patients who determined to be inappropriate

研究者

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