临床试验/ACTRN12615001244594

ACTRN12615001244594已完成未知

Comparative physiological evaluation with diaphragmatic ultrasound of the application of oxygen-therapy through a Venturi mask or a nasal high-flow device in patients recovering from severe exacerbation of chronic respiratory failure.

Federico Longhini, MD0 个研究点目标入组 30 人开始时间: 2015年11月12日最近更新: 2020年1月13日

适应症

试验速览

阶段: 未知
状态: 已完成
发起方
入组人数: 30

研究概览研究设计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
分配方式: Randomised controlled trial
主要目的: Treatment
盲法: Open (masking not used)

入排标准

年龄范围: 18 Years 至 o limit（—）
性别: All

入选标准

•All the patients meeting the following criteria will be eligible for the study: 1) age equal or greater than 18 years; 2) presence of consciousness; 3) previous NIV for at least 24 hours due to SE-CRF; 4) pH greater than 7.34; 5) respiratory rate (RR) less than or equal to 30 breaths/min.

排除标准

•Patients will be excluded if they meet one or more of the following criteria:
•1.refusal of patient's consent;
•2.Hemodynamic instability, as defined by a systolic blood pressure < 90 mmHg despite volemic optimizationn, or use of vasoactive agents, i.e. vasopressin or epinephrine at any dosage, norepinephrine > 0.2 mcg/kg/min, dopamine or dobutamine > 5 mcg/kg/min;
•3.major cardiac arrhythmia or electrographic signs of ischemia;
•4.use of accessory muscles with dyspnoea;
•5.pregnancy.
•The protocol will be interrupted if:
•1.agitation or mental status alteration
•2.increase use of accessory muscles and/or dyspnoea
•3.pH < 7.30
•4.systolic blood pressure < 90 mmHg
•5.onset of new cardiac arrhythmia

研究者

发起方

Federico Longhini, MD

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