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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
Washington University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Malnutrition, Child

Eligibility Criteria

6 Months - 59 Months (Child)All SexesDoes not accept healthy volunteers

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

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
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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
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Effect of an Alternative RUTF on Intestinal Permeability in Children With Severe Acute Malnutrition

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