ACTRN12616001101471已完成不适用
Efficacy of using intestinal permeability as a tool to monitor clinical progress in the critically ill
a Trobe University0 个研究点目标入组 40 人开始时间: 2016年8月15日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 40
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
- Non-randomised trial
- 主要目的
- Diagnosis
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •Adult patients aged greater than or equal to 18 years;
- •- Patients receiving or suitable for enteral feeding;
- •- Likely to be admitted to the ICU for greater than or equal to 3 days;
- •- Likely to require mechanical ventilation for > 24 hours;
- •- Patients with an indwelling catheter in situ;
- •- Patients receiving inotropic or vasopressor support at time of enrolment.
排除标准
- •- A past history of gut abnormalities, abdominal surgery within 2 years of ICU admission or malabsorption syndromes;
- •- Presenting condition or past history of abdominal trauma within 2 years of admission;
- •- Patients treated with therapeutic hypothermia during admission;
- •- Patients requiring continuous renal replacement therapy;
- •- Patients treated with non-steroidal anti-inflammatory drugs;
- •- Any situation where lactulose or any of the test sugars are used as part of the treatment plan;
- •- Patients receiving total parenteral nutrition or enteral feeding directly into the small bowel;
- •- Patients receiving or received chemotherapy or radiotherapy in the past 6 months;
- •- Pregnancy;
- •- When participation in the study is not believed to be in the best interest of the patient as determined by the treating physician.
研究者
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