Clinical Trial

Iron Absorption From Lipid-Based Nutrient Supplements

Active, Not Recruiting
View on ClinicalTrials.gov →
Summary
The overall objective of this study is to determine dietary iron absorption from lipid-based nutrient supplements (LNS) in apparently healthy and undernourished children. This case-control study will recruit apparently healthy children and children with uncomplicated undernutrition (age 1-3 years, n=15/group) from Msambweni and the surrounding rural communities in Kwale County, Kenya. At the baseline visit (day 0), participants will be provided with an LNS labeled with a stable iron isotope (57-Fe). Participants will return to the hospital 14 days later (day 14) for a blood draw. Blood collected on day 14 will be used to measure iron isotope incorporation into red blood cells. Blood collected at screening will be used to measure indicators of anemia, iron status, hepcidin, and inflammation.
Protocol Amendment History 2 changes
notable Primary completion pushed: 2026-03-01 -> 2027-01-01 2026-08-04
minor Completion pushed: 2026-03-01 -> 2027-01-01 2026-08-04
Trial Details
NCT Number NCT06870201
Lead Sponsor Pennington Biomedical Research Center
Collaborators: Jomo Kenyatta University of Agriculture and Technology
Conditions Undernutrition, Healthy
Enrollment 30 participants
Start Date 2025-03-25
Primary Completion 2027-01-01 (estimated)
Study Completion 2027-01-01 (estimated)
Updated on ClinicalTrials.gov 2026-08-03