Immunonutrition Supplementation for Improved Burn Wound Healing in Older Adults

Status: Terminated
Location: See location...
Intervention Type: Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This pilot study aims to assess the feasibility of providing immunonutrition supplementation to older burn patients (age 55 and older) and its impact on burn wound healing. Supplements containing arginine and omega 3 fatty acids have been shown to have beneficial effects on healing in other types of wounds but data within the burn population remains limited. 20 participants will be randomized into two arms, immunonutrition or conventional supplement and can expect to be on study for 3 months.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 55
Healthy Volunteers: f
View:

• Subject has partial of full thickness thermal injury of 1-15% of total body surface area (TBSA)

• Subject has an inpatient admission for their burn

• Subject or authorized decision maker understands the study procedures and can provide informed consent to participate in the study and authorization for release of relevant protected health information to the study investigator

Locations
United States
Wisconsin
University of Wisconsin
Madison
Time Frame
Start Date: 2022-07-01
Completion Date: 2024-09-09
Participants
Target number of participants: 11
Treatments
Experimental: Immunonutrition
Participants will consume a 6oz immunonutrition drink 2 times daily for 7 days and then once a day for remaining hospital stay.
Active_comparator: Conventional Supplement
Participants will consume a 6oz conventional supplement drink 3 times daily for 7 days and then once a day for remaining hospital stay.
Sponsors
Leads: University of Wisconsin, Madison

This content was sourced from clinicaltrials.gov