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Personalized Nutrition to Improve Recovery in Trauma (SeND Home)

Primary Purpose

Abdominal Trauma

Status
Not yet recruiting
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Nutrition Supplement
Sponsored by
Duke University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Abdominal Trauma focused on measuring precision nutrition, critical care, trauma, parenteral nutrition, indirect calorimetry

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: 18+ 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 Exclusion Criteria: 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.

Sites / Locations

  • Duke University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

SeND Home Pathway

Standard Nutrition

Arm Description

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.

Standard nutrition as determined by clinical providers.

Outcomes

Primary Outcome Measures

Change in six-minute walk distance (6 MWD)
Change in 6MWD from baseline to day 14 or hospital discharge will be compared between the two study arms

Secondary Outcome Measures

Change in physical function
This will be measured by comparing the changes in physical function tests (4 meter walk, sit-to-stand) between the two study arms.
Change in muscle strength
This will be measured by comparing the changes in grip and quad strength tests between the two study arms.
Change in muscle mass
This will be measured by comparing changes in bioelectrical impedance analysis (BIA) between the two study arms.
Change in Quality of Life (QoL)
This will be measured by comparing changes in the EuroQoL-5 Dimension and 43-item Trauma Specific Quality of Life measurement between the two study arms.
Change in cognition
This will be measured by looking at changes in mental health and cognition via questionnaires.
Infection
This will be measured by looking at the number of infections reported.
Length of Hospital/ICU stay
This will be measured by recording the length of hospital stay noted in the medical record.
Mortality rate
This will be measured by survival after 6 months.
Change in muscle mitochondrial metabolism
This will be measured by doing urine and blood tests.
Change in key resilience and inflammation biomarkers
This will be measured utilizing the Duke Pepper Panel which serves as a comprehensive set of biological indicators typically incorporating: hormones, inflammatory markers and genomic factors.

Full Information

First Posted
September 27, 2023
Last Updated
September 27, 2023
Sponsor
Duke University
Collaborators
United States Department of Defense, Baxter Healthcare Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT06065202
Brief Title
Personalized Nutrition to Improve Recovery in Trauma
Acronym
SeND Home
Official Title
Personalized Targeted Nutrition Via StructurEd Nutrition Delivery Pathway to Improve Recovery of Physical Function in Trauma
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
October 1, 2023 (Anticipated)
Primary Completion Date
March 30, 2024 (Anticipated)
Study Completion Date
June 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Duke University
Collaborators
United States Department of Defense, Baxter Healthcare Corporation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Abdominal Trauma
Keywords
precision nutrition, critical care, trauma, parenteral nutrition, indirect calorimetry

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
SeND Home Pathway
Arm Type
Experimental
Arm Description
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.
Arm Title
Standard Nutrition
Arm Type
No Intervention
Arm Description
Standard nutrition as determined by clinical providers.
Intervention Type
Dietary Supplement
Intervention Name(s)
Nutrition Supplement
Other Intervention Name(s)
CLINIMIX E 8/14 sulfite-free, CLINOLIPID 20%, Nutritional shakes
Intervention Description
Total parenteral nutrition (TPN) will be administered within 72 hours of abdominal surgery. Nutritional shakes will be started with a liquid diet and given 3 times a day. This will continue for 4 weeks after discharge.
Primary Outcome Measure Information:
Title
Change in six-minute walk distance (6 MWD)
Description
Change in 6MWD from baseline to day 14 or hospital discharge will be compared between the two study arms
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Change in physical function
Description
This will be measured by comparing the changes in physical function tests (4 meter walk, sit-to-stand) between the two study arms.
Time Frame
baseline, day 14 or hospital discharge, 3 and 6 months post-hospital discharge
Title
Change in muscle strength
Description
This will be measured by comparing the changes in grip and quad strength tests between the two study arms.
Time Frame
baseline, hospital discharge, 3 and 6 months post-hospital discharge
Title
Change in muscle mass
Description
This will be measured by comparing changes in bioelectrical impedance analysis (BIA) between the two study arms.
Time Frame
baseline, hospital discharge, 3 and 6 months post-hospital discharge
Title
Change in Quality of Life (QoL)
Description
This will be measured by comparing changes in the EuroQoL-5 Dimension and 43-item Trauma Specific Quality of Life measurement between the two study arms.
Time Frame
baseline, 3 and 6 months post-hospital discharge
Title
Change in cognition
Description
This will be measured by looking at changes in mental health and cognition via questionnaires.
Time Frame
baseline, 3 and 6 months post-hospital discharge
Title
Infection
Description
This will be measured by looking at the number of infections reported.
Time Frame
hospital discharge, 3 and 6 months post-hospital discharge
Title
Length of Hospital/ICU stay
Description
This will be measured by recording the length of hospital stay noted in the medical record.
Time Frame
hospital discharge
Title
Mortality rate
Description
This will be measured by survival after 6 months.
Time Frame
6 months post-hospital discharge
Title
Change in muscle mitochondrial metabolism
Description
This will be measured by doing urine and blood tests.
Time Frame
admission, day 14, and hospital discharge
Title
Change in key resilience and inflammation biomarkers
Description
This will be measured utilizing the Duke Pepper Panel which serves as a comprehensive set of biological indicators typically incorporating: hormones, inflammatory markers and genomic factors.
Time Frame
admission, day 14, and hospital discharge

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18+ 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 Exclusion Criteria: 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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Krista Haines, MD
Phone
919-681-3784
Email
krista.haines@duke.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Shauna Howell
Phone
919-613-1588
Email
shauna.eggertson@duke.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paul Wischmeyer, MD
Organizational Affiliation
Duke
Official's Role
Principal Investigator
Facility Information:
Facility Name
Duke University Hospital
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27710
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shauna Howell
Phone
919-668-3771
Email
shauna.eggertson@duke.edu
First Name & Middle Initial & Last Name & Degree
Krista Haines, MD

12. IPD Sharing Statement

Plan to Share IPD
No

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Personalized Nutrition to Improve Recovery in Trauma

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