NL-OMON50646尚未招募不适用
CONvalescence of FUnCtional outcomes after ICU Stay by oral protein supplementation The CONFUCIUS oral protein supplementation trial - CONFUCIUS oral protein supplementation trial
Ziekenhuisvoorzieningen Gelderse Vallei0 个研究点目标入组 72 人开始时间: 待定最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 72
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
- 18 至 99（—）
入选标准
- •1. Age >= 18 years
- •2. Living at home before hospital admission
- •3. Minimum ICU stay of 72 h
- •4. Informed consent
排除标准
- •1. MRC sum score <= 24 or 48 >= at ICU discharge
- •2. Barthel Index <14 before ICU admission
- •3. Allergy/intolerance for study product
- •4. Serum creatinin > 173 mcmol/l (renal dysfunction)
- •5. Inclusion in other intervention trial since ICU admission
- •6. Inflammatory Bowel Disease
- •7. Zwangerschap
- •8. Underlying disease in which in the eyes of the attending physician, the
- •protein or carbohydate supplement could form a risk for the patient
研究者
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