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Study identifier: NCT06521086 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Optimizing Recovery in Trauma Patients by Integrating Enhanced Nutrition Delivery

Condition: Trauma · Critical Illness  ·  Sponsor: Duke University

PhaseNA
Planned participants60
Who can joinAll sexes, 45 Years to no upper limit
Healthy volunteersNo

About this study

This is a prospective, randomized, controlled trial designed to evaluate the impact of enhanced protein supplementation compared to a standard of care nutrition delivery in critically ill older adult trauma patients. Subjects will be randomized 1:1 to either enhanced nutrition or control arm. Subjects randomized to the enhanced nutrition arm will receive oral nutrition supplements (ONS) up to 3 times per day while in the hospital and for 4 weeks after discharge. Subjects in the standard of care arm will receive normal nutrition recommendations from their clinical providers. Participants in both groups will undergo non-invasive tests that measure how much energy (calories) they are using, body composition, and muscle mass.

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

Talk to the study team

Paul Wischmeyer, MD  ·  919-681-9660  ·  paul.wischmeyer@duke.edu

Krista Haines, MD  ·  919-681-3784  ·  krista.haines@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/NCT06521086