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临床试验/NCT00318331
NCT00318331终止2 期

Randomized Clinical Trial Comparing Enteral Glutamine Supplementation to Standard of Care Enteral Feeding in Critical Illness

Christiana Care Health Services1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2006年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
终止
入组人数
20
试验地点
1
主要终点
Mortality

研究概览

简要总结

Glutamine is an amino acid which is rapidly depleted in critical illness. It is used as energy by cells that line the gut, vital for immune system function, and works as an anti-oxidant. Glutamine supplementation has been shown to improve outcomes in ICU patients. We hypothesize that critically ill patients given extra glutamine will have less of an inflammatory response and therefore better outcomes than patients not given extra glutamine. Our study randomizes patients to tube feeding with OR without extra glutamine to see if it affects patient outcomes as well as markers of inflammation.

详细描述

Glutamine, a nonessential amino acid, is preferred fuel for rapidly proliferating cells in human body. Those cells include the enterocytes in small intestine, lymphocytes, macrophages, and fibroblasts. Glutamine also transports nitrogen between tissues and serves as a precursor to glutathione which is a potent antioxidant. A healthy human body contains abundant glutamine, either from diet or from skeletal muscle tissue that synthesizes it.

During critical illness the demand for glutamine is increased. Rapid depletion of glutamine stores in critically ill patients has been described and correlated to increased mortality. Glutamine depletion may be deleterious in critical illness because of adverse effects on the essential functions mentioned above. For example glutamine depletion may cause gut mucosal barrier function to deteriorate, leading to bacterial translocation and enhanced systemic inflammatory response with increased risk for multisystem organ failure. Clinical trials performed in a wide range of patients with serious illness, including cancer, trauma, burn, major surgery and critical illness, have demonstrated possible benefits of glutamine supplementation. Interpretation of the results of multiple studies is made difficult based on differences in glutamine dosing, route of administration, population studied, and endpoints used.

Blood volume analysis has been shown to be a good measure of capillary leak. The DAXOR blood volume analyzer kit was recently approved by the FDA for blood volume analyses and also has the capacity of measuring capillary permeability by looking at the slope of albumin transudation. It is a simpler way to measure capillary permeability than other methods described.

Reviewing the previous study results, glutamine supplementation in parental form and with higher dose in various patient populations has shown evidence of being beneficial. Studies of enteral glutamine therapy have also showed benefits, but results are less consistent possibly because of the heterogeneous study methodology described above. Moreover, most of the studies are carried out in burn patients and surgical patients; there were few studies in critical ill medical patients. Finally no study has specifically looked at the mechanism via which glutamine has conferred protection.

Comparison: Critically ill patients given enteral tube feeds compared to critically ill patients given enteral tube feeds with supplemental glutamine.

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, Investigator, Outcomes Assessor)

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

  • Admission to MICU/ CICU
  • Age greater than or equal to 18 years old
  • Requirement for enteral nutrition
  • Presence or planned insertion of central venous catheter as part of routine medical care
  • Requirement for mechanical ventilation
  • APACHE II Score >/= 15

排除标准

  • Female of child-bearing age (i.e. less than 45 years old)
  • Enteral nutrition begun prior to randomization
  • Receiving Total Parenteral Nutrition
  • Requirement for protein restriction
  • Creatinine >4 mg/dl
  • History of cirrhosis and/or clinical signs of heptic encephalopathy

研究组 & 干预措施

A

Active Comparator

Will receive enteral glutamine

干预措施: Glutamine (Drug)

结局指标

主要结局

Mortality

时间窗: 28 days

Length of ICU stay

时间窗: 28 days

Number of Ventilator Days

时间窗: 28 days

Number of days receiving antibiotics

时间窗: 28 days

次要结局

  • Change in CRP(72 hours)
  • Change in APACHE Score(72 hours)
  • Change in Number of SIRS Criteria(72 hours)
  • Change in Capillary Leak as measured by blood volume analysis(72 hours)
  • Correlation between capillary permeability and APACHE Score(72 hours)
  • Correlation between capillary permeability and Mortality(72 hours)

研究者

申办方类型
Other

研究点 (1)

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