Optimizing Recovery in Trauma Patients by Integrating Enhanced Nutrition Delivery

Recruiting N/A Interventional Study
Trauma Critical Illness
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
45 and older
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
60 (estimated)
Sponsor
Duke University · Other
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About This Trial
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 ti…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patients who are at least 45 years old and presented to the Emergency Department as a leveled trauma * Patients who have the ability to tolerate oral nutrition * Patients who have had a standard of care CT scan this admission Exclusion Criteria: * Expected withdrawal of life…
Contacts

Paul Wischmeyer, MD

919-681-9660

paul.wischmeyer@duke.edu

CONTACT

Krista Haines, MD

919-681-3784

krista.haines@duke.edu

CONTACT