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临床试验/NCT00425529
NCT00425529已完成早期 1 期

Tolerance and Practicality of Module AOX - a Modular Device for Supplementation of Enteral Nutrition

Amsterdam UMC, location VUmc2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2002年2月1日最近更新:
适应症

试验速览

阶段
早期 1 期
状态
已完成
发起方
入组人数
20
试验地点
2
主要终点
Tolerance: stool outcome (frequency, consistency), diarrhea, faltulence, abdominal pain, amount of feeding according to goal, changes of amount fed, discontinuation of feeding

研究概览

简要总结

The primary objective of this clinical trial is to test the tolerance and practicality of the new device Module AOX.

The secondary objective is to determine the changes in oxidative, antioxidative status, plasma free amino acids, and various immune parameters in critically ill patients receiving the enteral nutrition with and without using Module AOX.

详细描述

Surgery and trauma induce hypercatabolism accompanied by a systemic immunoinflammtory response and massive production of reactive oxygen species at the site of injury. In these situations, requirements for certain amino acids (glutamine, cysteine) and antioxidant micronutrients (zinc, vitamin E, vitamin C, beta-caroteen, selenium) are markedly increased and may not be covered by the levels normally present in standard enteral diets, especially in the early phase when enteral nutrition is introduced gradually. Thus, supplementation with amino acids and antioxidant micronutrients may be appropiate in order to optimize nutritional support in such patients.

The administration of selected nutrients via modular devices added to a standard enteral formulation is an attractive means of providing optimized nutrition support for specific disease states. Module AOX is intended for supplementation of patients requiring nutritional support for a condition in which oxidative stress is expected. The module contains:

  • Glutamine: to support gut mucosal and immune function, to minimize early depletion of glutamine stores and preserve body protein
  • Cysteine: to support synthesis of glutathione, an important cellular antioxidant, and to support the synthesis of acute phase proteins
  • Vitamin E, vitamin C and beta-caroteen: water- and lipid-soluble antioxidant micronutrients to boost antioxidant defenses
  • Zinc: to compensate for increased losses and to support protein synthesis, immune function and wound healing
  • Selenium: to compensate for increased losses, support antioxidant defenses and immune function

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patients who will undergo major surgery of esophagus, stomach or pancreas
  • patients who will be eligible for jejunostomy feeding
  • age >18 and <75 y
  • BMI < 35
  • having obtained his/her or his/her legal representative's informed consent

排除标准

  • patients with a history of main cardiovascular or kidney disease
  • weigth loss >10% during the last 6 months
  • patients who have received corticosteroids, or investigational drugs, in the last 6 weekd prior to surgery
  • patients with HIV infection
  • patients who are participating in another clinical trial

结局指标

主要结局

Tolerance: stool outcome (frequency, consistency), diarrhea, faltulence, abdominal pain, amount of feeding according to goal, changes of amount fed, discontinuation of feeding

Practicality: time for connecting the device to the pouch, time needing for mixing content of device with the content of the enteral feding pouch, clotting of theadministration set, product flow,leakage, clarity of instructions of usage

次要结局

  • vitamin C, Vitamin E. beta-caroteen, GSH/GSSG, cysteine/cystine, GPx, isoprostane, TAS, Zn, Se, plasma free amino acids, HLADR, TNF soluble receptors (55/75), LBP, BPI, IL-1 IR II, leptin, soluble leptin receptor, IL-6, IL-8, and microciological safety

研究者

发起方
Amsterdam UMC, location VUmc
申办方类型
Other

研究点 (2)

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