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临床试验/NCT01463878
NCT01463878终止4 期

Enteral Nutrition and Glycemic Variability NICU Study

Eastern Virginia Medical School2 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2011年11月最近更新:
适应症

试验速览

阶段
4 期
状态
终止
入组人数
14
试验地点
2
主要终点
Glycemic Variability

研究概览

简要总结

Primary Objective:

To determine the effects of a diabetes specific enteral formula compared to a standard formula supplemented with protein (isocaloric and isonitrogenous) on the mean blood glucose and glycemic variability in a homogenous group of critically ill patients in a neurological ICU. Blood glucose will be recorded every minute using a continuous blood glucose monitor. The primary end points will be the difference between the mean blood glucose levels and the glucose variability between the control and intervention groups for the time period that the patient is in the ICU and receiving tube feeds and for up to a maximum of 14 days.

Secondary Objectives:

To determine the effects of the diabetes specific versus standard tube feeds on the change in muscle thickness and volume measured by 2-dimensional ultrasound imaging during the patients ICU stay.

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
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 89 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients aged between 18 and 89 years old
  • Patients with critical illness including ischemic or hemorrhagic stroke, epidural/subdural bleeds and subarachnoid hemorrhage
  • Patients who are expected to stay in the ICU for at least 5 days
  • Hyperglycemia is not an inclusion criteria

排除标准

  • Patients who have received or will be treated with systemic corticosteroids.
  • Patients who will be receiving high doses of propofol (>40 cc/hr)
  • Patients with type 1 Diabetes
  • Patients with sepsis or acute trauma
  • Patients with an expected stay in the ICU of less than 4 days
  • Patients who are unable to receive enteral nutrition or who have medical conditions precluding nutrition by the enteral route including allergies to formula components
  • Pregnant and lactating patients
  • Patients with prior history of gastroparesis
  • Patients with acute kidney failure (creatinine > 2.5mg/dl)
  • Patients with acute liver failure (bilirubin > 2.0 mg/dl)

结局指标

主要结局

Glycemic Variability

时间窗: Entire ICU stay. Up to 14 days in the ICU (average about 7 days)

The patients blood glucose levels will be monitored with a continuous blood glucose monitor which records the calibrated blood glucose level every minute. The mean blood glucose over the patients entire ICU stay (up to 14 days) as well as the mathematical variation (fluctuation) in blood glucose levels will be calculated. The degree of glycemic variation will be assessed by a number of mathematical formula, including mean amplitude of glycemic excursions (MAGE). These parameters will be compared between the control and intervention groups.

次要结局

  • Quadriceps Muscle Volume(First versus last measurment in ICU. Up to 14 days (average 7 days))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Paul Marik

Chief of Pulmnary and Critical Care Medicine

Eastern Virginia Medical School

研究点 (2)

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