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临床试验/JPRN-UMIN000017792
JPRN-UMIN000017792已完成未知

Heliox inhalation therapy for Japanese pediatrics with respiratory distress and/or respiratory failure associated with acute bronchiolitis - historical control open study - Heliox inhalation therapy for pediatric severe acute bronchiolitis

agano Children's Hospital Division of anesthesiology0 个研究点目标入组 10 人开始时间: 2015年6月3日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
10

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
ot applicable 至 2years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1. Patients who have severe congenital heart diseases. 2. Patients who has severe chronic lung disease. 3. Patients who have severe malformation of bronchi or lung. 4. Patients who are diagnosed as bronchial asthma and under treatment. 5. Patients who have severe physiologic conditions continued more than 6 hours as follows. 1) OI>15cmH2O/mmHg 2) Mean arterial pressure<30mmHg 3) Heart rate>200bpm 6. Patients who have to use medical devices with hot wire flow sensor (exclude the device which is confirmed with Heliox). 7. Patients who are predicted that need Heliox inhalation more than 7 days. 8. Other patients who are identified as inappropriate for this study by the physicians in charge.

研究者

发起方
agano Children&#39;s Hospital Division of anesthesiology

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