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临床试验/NCT06065202
NCT06065202招募中2 期

Personalized Targeted Nutrition Via StructurEd Nutrition Delivery Pathway to Improve Recovery of Physical Function in Trauma

Duke University2 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2024年4月12日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
招募中
入组人数
150
试验地点
2
主要终点
Change in six-minute walk distance (6 MWD)

研究概览

简要总结

The purpose of this study is to determine if a particular method of providing nutrition improves the outcomes of patients in the intensive care unit (ICU) who have undergone abdominal surgery following trauma and would require nutrition delivered via the bloodstream (called total parenteral nutrition or TPN). The nutrition method being tested is a structured nutrition delivery plan, called the SeND Home pathway, that involves TPN, oral nutrition supplements, and the use of a device (called an indirect calorimeter or IC) to measure calorie needs. Participants will be randomly assigned (like the flip of a coin) to the SeND Home program or standard of care nutrition. In the SeND Home program, participants will receive TPN, followed by oral nutrition supplements (shakes) for 4 weeks after discharge. The control group will follow standard of care nutrition delivery that begins during ICU stay and concludes at hospital discharge. Participants in both groups will undergo non-invasive tests that measure how much energy (calories) they are using, body composition, and muscle mass and complete walking and strength tests, and surveys about quality of life.

详细描述

Severe abdominal trauma can impact patients in a variety of ways. Current data shows that trauma patients can experience problems with physical function, muscle weakness, and poor quality of life after they are released from the hospital. There is a critical need to improve nutrition in trauma patients with severe abdominal injuries to optimize the recovery process. The purpose of this study is to evaluate if the use of a planned nutrition delivery plan with early intravenous (IV) nutrition will improve outcomes. Participants will be randomly assigned 1:1, like flipping a coin, to the SeND Home program or routine care.

Participants in the standard of care program will receive standard nutrition delivery as determined by clinical care providers. This may include TPN.

Participants in the SeND Home program will receive TPN within 72 hours of abdominal surgery. Indirect calorimetry will be used to determine nutrition needs.Once participants are able to have a liquid diet they will receive nutrition shakes up to 3 times a day while in the hospital and for 4 weeks after discharge.

Participants will undergo tests to measure muscle mass, have blood draws, complete walking and strength tests, and surveys about quality of life. These tests will be done at several times throughout hospitalization and participants will be asked to return for a 3 month follow-up visit.

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
15 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 15+ years old
  • Penetrating abdominal trauma requiring emergent major abdominal surgery
  • Admitted to the surgical ICU
  • Not expected to receive oral nutrition for 72 hours or more

排除标准

  • Patients who are unable to ambulate at baseline
  • Expected withdrawal of life-sustaining treatment within 48 hours
  • Prisoners
  • Positive pregnancy test for women of child bearing potential.

研究组 & 干预措施

SeND Home Pathway

Experimental

Total parenteral nutrition (TPN) will begin within 72 hours of abdominal surgery. Calorie needs will be determined by indirect calorimetry. Nutritional shakes will begin when a liquid diet is started. These will be taken 3 times a day while in the hospital and for 4 weeks after discharge.

干预措施: Nutrition Supplement (Dietary Supplement)

Standard Nutrition

No Intervention

Standard nutrition as determined by clinical providers.

结局指标

主要结局

Change in six-minute walk distance (6 MWD)

时间窗: 3 months

Change in 6MWD from baseline to day 14 or hospital discharge will be compared between the two study arms

次要结局

  • Length of Hospital/ICU stay(hospital discharge)
  • Infection(hospital discharge, 3 and 6 months post-hospital discharge)
  • Change in physical function(baseline, day 14 or hospital discharge, 3 and 6 months post-hospital discharge)
  • Change in muscle strength(baseline, hospital discharge, 3 and 6 months post-hospital discharge)
  • Change in Quality of Life (QoL)(baseline, 3 and 6 months post-hospital discharge)
  • Change in cognition(baseline, 3 and 6 months post-hospital discharge)
  • Mortality rate(6 months post-hospital discharge)
  • Change in muscle mitochondrial metabolism(admission, day 14, and hospital discharge)
  • Change in muscle mass(baseline, hospital discharge, 3 and 6 months post-hospital discharge)
  • Change in key resilience and inflammation biomarkers(admission, day 14, and hospital discharge)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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