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临床试验/NCT02594865
NCT02594865已完成不适用

Glucerna in Critically Ill Patients (GluCip Trial): Investigating the Glycaemic Effects of a Reduced-carbohydrate, Modified-fat, Fiber-containing Enteral Formula (Glucerna®) in Critically Ill Patients.

PHJ van der Voort2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2015年9月1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
100
试验地点
2
主要终点
Glucose variability

研究概览

简要总结

To investigate whether the administration of Glucerna achieves less glycaemic variability, defined as the mean absolute glucose (MAG) change, and better glycaemic control compared to a standard high-carbohydrate enteral formula. Continuous glucose monitoring technology will be used to evaluate glycaemic variability and glycaemic control.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age ≥ 18 years;
  • Patients with an anticipated stay of at least 48 hours of admission to the intensive care
  • Expected to receive enteral feeding for at least 48 hrs
  • Indication for glucose regulation with insulin (according to the current glucose treatment protocol)
  • Patient or surrogate understands and signs informed consent document.

排除标准

  • Patients with pre-existing contraindications to enteral feeding or to placement of a continuous glucose monitoring system
  • Patients previously randomised into the GluCip trial
  • Any disease or condition which the investigator or treating physician feels would interfere with the trial or the safety of the patient.

结局指标

主要结局

Glucose variability

时间窗: 72 hours

The primary outcome is the extent of glucose variability, defined as the mean absolute glucose (MAG) change (delta glucose/delta time) in mmol/l/hr.

次要结局

  • Amount of insulin use(72 hours)
  • Duration of severe hypoglycemic events(72 hours)
  • Number of severe hypoglycemic events(72 hours)
  • Mean glucose and standarddeviation(72 hours)
  • Duration of severe hyperglycemic events(72 hours)
  • Daily calorie administration(72 hours)
  • Daily nutrient administration(72 hours)
  • Time in target range(72 hours)
  • Number of severe hyperglycemic events(72 hours)

研究者

发起方
PHJ van der Voort
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

PHJ van der Voort

Prof., MD, PhD, MSc

Onze Lieve Vrouwe Gasthuis

研究点 (2)

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