Effect of an Alternative RUTF on Intestinal Permeability in Children With Severe Acute Malnutrition
Primary Purpose
Malnutrition, Child
Status
Completed
Phase
Not Applicable
Locations
Sierra Leone
Study Type
Interventional
Intervention
S-RUTF
oat RUTF
Sponsored by
About this trial
This is an interventional treatment trial for Malnutrition, Child
Eligibility Criteria
Inclusion Criteria:
- mid-upper arm circumference (MUAC) <11.5 cm
Exclusion Criteria:
- Children currently involved in another research trial or feeding program
- Children developmentally delayed
- have a chronic debilitating illness
- history of peanut or milk allergy
Sites / Locations
- Project Peanut Butter
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
S-RUTF
oat-RUTF
Arm Description
Children will receive approximately 175 kcal/kg/d of standard ready to use therapeutic food which provides a full daily doses of vitamins and micronutrients. Caregivers will instruct caregivers to feed the supplement only to the enrolled child.
Children will receive approximately 175 kcal/kg/d of oat ready-to-use therapeutic food which provides a full daily doses of vitamins and micronutrients. Caregivers will instruct caregivers to feed the supplement only to the enrolled child.
Outcomes
Primary Outcome Measures
Change of % of lactose excreted between enrollment and 4 weeks after enrollment
%L measured in the urine relative to the amount ingested will be calculated for children in both groups. %L will be categorized as normal (<0.2%) and abnormal (>0.2)
Secondary Outcome Measures
fecal 16S rRNA configuration after 4 weeks of feeding
Multi amplicon rRNA characterization of flash frozen stool sample
Full Information
NCT ID
NCT04334538
First Posted
March 30, 2020
Last Updated
August 5, 2022
Sponsor
Washington University School of Medicine
Collaborators
Project Peanut Butter, Sierra Leone, Ministry of Health and Sanitation, Sierra Leone
1. Study Identification
Unique Protocol Identification Number
NCT04334538
Brief Title
Effect of an Alternative RUTF on Intestinal Permeability in Children With Severe Acute Malnutrition
Official Title
Effect of an Alternative RUTF on Intestinal Permeability in Children With Severe Acute Malnutrition
Study Type
Interventional
2. Study Status
Record Verification Date
August 2022
Overall Recruitment Status
Completed
Study Start Date
March 2, 2021 (Actual)
Primary Completion Date
September 6, 2021 (Actual)
Study Completion Date
September 6, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Washington University School of Medicine
Collaborators
Project Peanut Butter, Sierra Leone, Ministry of Health and Sanitation, Sierra Leone
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Ready-to-use therapeutic food (RUTF) is the standard of care for the treatment of SAM. UNICEF requires that there be no oil separation in these products necessitating the use of emulsifiers. The effect of emulsifiers on gut health and integrity in children receiving an exclusive diet of RUTF is unknown. The PIs have recently completed a randomized, triple-blind, controlled, clinical equivalency trial in Sierra Leone comparing the alternative oat RUTF (oat-RUTF) to standard RUTF on recovery rates in children with SAM. This study demonstrated higher rates of recovery among children receiving the oat-RUTF. The investigators hypothesize that this benefit may be due to the lack of emulsifier in the oat-RUTF resulting in improved intestinal health.This research project is a double-blind, randomized, controlled clinical effectiveness trial comparing a novel RUTF containing oats and no emulsifier and standard RUTF on recovery from severe acute malnutrition (SAM) and effects on intestinal health. The trial will be conducted in up to 40 PHUs in Western Rural and Pujehun Districts where supplementary feeding programs (SFP) are not currently available.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malnutrition, Child
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
129 (Actual)
8. Arms, Groups, and Interventions
Arm Title
S-RUTF
Arm Type
Active Comparator
Arm Description
Children will receive approximately 175 kcal/kg/d of standard ready to use therapeutic food which provides a full daily doses of vitamins and micronutrients. Caregivers will instruct caregivers to feed the supplement only to the enrolled child.
Arm Title
oat-RUTF
Arm Type
Experimental
Arm Description
Children will receive approximately 175 kcal/kg/d of oat ready-to-use therapeutic food which provides a full daily doses of vitamins and micronutrients. Caregivers will instruct caregivers to feed the supplement only to the enrolled child.
Intervention Type
Dietary Supplement
Intervention Name(s)
S-RUTF
Intervention Description
Children will receive approximately 175 kcal/kg/d of standard ready-to-use therapeutic food which provides a full daily doses of vitamins and micronutrients. Caregivers will instruct caregivers to feed the supplement only to the enrolled child.
Intervention Type
Dietary Supplement
Intervention Name(s)
oat RUTF
Intervention Description
Children will receive approximately 175 kcal/kg/d of oat ready-to-use therapeutic food which provides a full daily doses of vitamins and micronutrients. Caregivers will instruct caregivers to feed the supplement only to the enrolled child.
Primary Outcome Measure Information:
Title
Change of % of lactose excreted between enrollment and 4 weeks after enrollment
Description
%L measured in the urine relative to the amount ingested will be calculated for children in both groups. %L will be categorized as normal (<0.2%) and abnormal (>0.2)
Time Frame
at week 4 after enrollment
Secondary Outcome Measure Information:
Title
fecal 16S rRNA configuration after 4 weeks of feeding
Description
Multi amplicon rRNA characterization of flash frozen stool sample
Time Frame
after 4 weeks of feeding
10. Eligibility
Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
59 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
mid-upper arm circumference (MUAC) <11.5 cm
Exclusion Criteria:
Children currently involved in another research trial or feeding program
Children developmentally delayed
have a chronic debilitating illness
history of peanut or milk allergy
Facility Information:
Facility Name
Project Peanut Butter
City
Pujehun
Country
Sierra Leone
12. IPD Sharing Statement
Citations:
PubMed Identifier
36055798
Citation
Hendrixson DT, Naskidashvili N, Stephenson KB, Laury ML, Koroma AS, Manary MJ. An Alternative Oat-Containing, Ready-To-Use, Therapeutic Food Does Not Alter Intestinal Permeability or the 16S Ribosomal RNA Fecal Microbiome Configuration Among Children With Severe Malnutrition in Sierra Leone: A Randomized Controlled Trial. J Nutr. 2023 Jan 14;152(12):2744-2753. doi: 10.1093/jn/nxac207.
Results Reference
derived
Learn more about this trial
Effect of an Alternative RUTF on Intestinal Permeability in Children With Severe Acute Malnutrition
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