Safety Efficacy, and Cost-effectiveness of Modified Doses of Ready-to-use Therapeutic and Supplementary Foods for the Treatment of Moderate Acute Malnutrition Among Children 6-59 Months of Age in Ethiopia

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Protocols for the community-based management of acute malnutrition (CMAM) have not changed significantly for more than 20 years, with relatively complex treatment protocols and persistent supply chain challenges that have limited overall program coverage, leaving millions of malnourished children without care annually. The overarching goal of this research project is to simultaneously test two novel simplified approaches in CMAM with potential to improve program coverage. The simplified approach includes two parallel clinical trials for SAM and MAM treatment. Two fixed-dose regimes of RUTF will be tested against the current fixed-dose regimen of RUSF for children with MAM.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 6 months
Maximum Age: 4
Healthy Volunteers: f
View:

• Age 6-59 months

• Reside in the catchment area of the health post where the trial is to be conducted without plans to leave the area over the next year

• Uncomplicated moderate acute malnutrition, as defined by no signs of severe illness that would require referral to inpatient facility

• Pass appetite test conducted at the time of enrollment

• Consent for randomization into the study given by mother, father, and/or other primary caregiver

• Mid-upper arm circumference of 115-124 mm without nutritional edema

• Weight-for-height Z-score (WHZ) between -2 and -3

Locations
Other Locations
Ethiopia
Gode
RECRUITING
Gode
Sekota
NOT_YET_RECRUITING
Sekota
Teltele
RECRUITING
Teltelē
Contact Information
Primary
Indi Trehan, MD MPH DTM&H
itrehan@uw.edu
+12067696068
Time Frame
Start Date: 2023-09-25
Estimated Completion Date: 2026-09-25
Participants
Target number of participants: 2400
Treatments
Active_comparator: Control Group
1 sachet (535 kcal) of RUSF per day
Experimental: MAM Experimental A
1 sachet (500 kcal) of RUTF per day
Experimental: MAM Experimental B
2 sachets (1000 kcal) of RUTF per day
Related Therapeutic Areas
Sponsors
Collaborators: University of Washington, Ethiopian Public Health Institute
Leads: Action Against Hunger USA

This content was sourced from clinicaltrials.gov