跳至主要内容
临床试验/NCT01877850
NCT01877850已完成不适用

Non Pharmacological Randomized Clinical Trial Designed to Evaluate the Difference of the Duration of Weaning Process From the Ventilator Between Protocol-driven Weaned Patients and Clinical-driven Weaned Patients.

ELENA PELI,MD1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2013年5月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
60
试验地点
1
主要终点
duration of weaning

研究概览

简要总结

The purpose of this study is to evaluate the difference of the duration of weaning process from the ventilator between protocol-driven weaned patients and clinical judgment driven weaned patients.

详细描述

All patients with prolonged weaning and who required tracheostomy are enrolled in the study. These patients are randomized as "Case or Control" by a computer program.

Patients can start the weaning process when the acute phase of the respiratory failure has been resolved and pressure support ventilation was setted.

For all this patients are calculated modified-BWAP(BWAP-M) and TOBIN indexes. The "Case" patients started the weaning protocol process only if BWAP-M value is more than 15 or BWAP-M 10-15 with Tobin index < 100.

If not, the BWAP-M and Tobin will be calculated every day. The Control patients will start weaning by clinical judgement even if the BWAP-M value is less than 10.

For all patients are calculated: the duration of weaning process, the ICU length of stay and the duration of the mechanical ventilation.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • all patients that are clinically identified as prolonged to wean (failed 3 spontaneous breathing trials or 7 days or more of mechanical ventilation after the initial unsuccessful trial) and tracheostomized in ICU
  • improvement or resolution of the underlying causes of acute respiratory failure ratio between pressure partial artery of oxygen and fraction inspired oxygen (PaO2/FiO2) >200 with fraction inspired oxygen (FiO2)< 0,
  • pressure supported ventilation at the time of enrollment.

排除标准

  • patients assessed as easy weaning and not tracheostomized;
  • patients already tracheostomized on admission to ICU.

结局指标

主要结局

duration of weaning

时间窗: within the first 15 days (plus or minus 5 days) after start of weaning

次要结局

  • duration of mechanical ventilation(within the first 12 days (plus or minus 10 days) after start of mechanical ventilation)

研究者

发起方
ELENA PELI,MD
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

ELENA PELI,MD

dirigente medico

Università degli Studi di Brescia

研究点 (1)

Loading locations...

相似试验