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临床试验/ISRCTN82559457
ISRCTN82559457已完成未知

Comparison of an automated weaning programme and a standard clinical weaning protocol for weaning critically ill patients: a randomised controlled trial

Guy's and St. Thomas' NHS Foundation Trust (UK)0 个研究点目标入组 500 人开始时间: 2005年9月30日最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
500

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

性别
All

入选标准

  • Added as of 10/12/2007:
  • Major entry criteria (suspected or proven infection, presence of a systemic response to the infection within the 48-hour period immediately preceding enrolment into the study, have or have had one or more sepsis-induced organ failures within the 48-hour period immediately preceding enrolment into the study).
  • 1. Age >=18 years
  • 2. Acute Physiology and Chronic Health Evaluation II (APACHE II) score =10
  • 3. Precipitating injury (surgery, trauma, hypovolemia, episode of infection or sepsis) occurred within the last 48 hours before Intensive Care Unit (ICU) entry
  • 4. Expected Length Of Stay (LOS) in the ICU >3 days
  • 5. Indication for enteral nutrition for 5-10 days
  • 6. Start of nutritional therapy with Intestamin or control supplement within 24 hours after inclusion criteria are fulfilled

排除标准

  • 1. Under 18 years of age
  • 2. Requirement for high doses of vasopressor
  • 3. Body temperature greater than 39ºC or less than 36ºC
  • 4. GCS = 12 without or with minimal sedation
  • 5. 'Do Not Resuscitate' order or expected short term prognosis
  • 6. Patients chronically ventilated at home with tracheostomy
  • 7. Patients with primary neurological cause of ventilator dependence
  • 8. Pregnancy
  • 9. Prolonged cardiac arrest with poor neurological prognoses
  • 10. Inability to obtain consent from patient or legal representative

研究者

发起方
Guy's and St. Thomas' NHS Foundation Trust (UK)

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