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Study identifier: NCT06065202 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Personalized Nutrition to Improve Recovery in Trauma

Condition: Abdominal Trauma  ·  Sponsor: Duke University

PhasePhase 2
Planned participants150
Who can joinAll sexes, 15 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Krista Haines, MD  ·  919-681-3784  ·  krista.haines@duke.edu

Hilary Winthrop  ·  919-668-7238  ·  hilary.winthrop@duke.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Duke University HospitalDurham, North Carolina, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06065202