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Changes in Microbiota and Iron Status After Iron Fortification of Complementary Foods

Primary Purpose

Bacterial Infections

Status
Completed
Phase
Not Applicable
Locations
Kenya
Study Type
Interventional
Intervention
fortification with iron and micronutrients
Sprinkles
Sponsored by
Swiss Federal Institute of Technology
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Bacterial Infections

Eligibility Criteria

24 Weeks - 28 Weeks (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Mother at least ≥15 years of age, infants 5.5- 6.5 months
  • Willingness to provide informed consent
  • Apparent good health
  • Long-term residence in study site and anticipating residing in the area for at least 3 years
  • Speak a Mjikenda language or Kiswahili in the home
  • Willingness to provide blood samples during clinic visits

Exclusion Criteria:

  • Hemoglobin <70 g/L for infants; these infants will be referred for treatment at the local health clinic/hospital.
  • Acute or chronic pulmonary, cardiovascular, hepatic, renal or neurological condition or any other finding that in the opinion of the PI or co-researchers that would increase risk of participating in the study.
  • Other conditions that in the opinion of the PI or co-researchers would jeopardize the safety or rights of a participant in the trial or would render the participant unable to comply with the protocol

Sites / Locations

  • Kikoneni Clinic

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Placebo Comparator

Experimental

Placebo Comparator

Arm Label

MixMe powder (iron & micronutrients)

MixMe powder (micronutrients, no iron)

Sprinkles (iron and micronutrients)

Sprinkles (micronutrients, no iron)

Arm Description

Vitamin A 300 µg; Vitamin C 30 mg; Folic Acid 160 µg; Iron 12.5 mg; Zinc 5 mg

Vitamin A 300 µg; Vitamin C 30 mg; Folic Acid 160 µg; Zinc 5 mg

Outcomes

Primary Outcome Measures

gut microbiota composition
Changes in gut microbiota composition

Secondary Outcome Measures

iron status
Efficacy of iron fortification in complementary foods

Full Information

First Posted
April 23, 2010
Last Updated
June 6, 2013
Sponsor
Swiss Federal Institute of Technology
Collaborators
University of KwaZulu, University of Nairobi
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1. Study Identification

Unique Protocol Identification Number
NCT01111864
Brief Title
Changes in Microbiota and Iron Status After Iron Fortification of Complementary Foods
Official Title
The Effect of Iron Fortification of Complementary Foods on Iron Status and Infant Gut Microbiota in Kenya
Study Type
Interventional

2. Study Status

Record Verification Date
June 2013
Overall Recruitment Status
Completed
Study Start Date
February 2010 (undefined)
Primary Completion Date
September 2012 (Actual)
Study Completion Date
October 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Swiss Federal Institute of Technology
Collaborators
University of KwaZulu, University of Nairobi

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Infants and children under two years are the group with the highest rates of iron deficiency anemia. Provision of sufficient dietary iron to this age group is a challenge, and in-home iron fortification of complementary foods using micronutrient powders can be an effective approach. However, WHO has recently cautioned against untargeted use of in-home micronutrient powders that contain the entire iron RDA for a child in a single dose in areas with high rates of infections from malaria and diarrheal disease. Therefore, in this study, we will investigate the effect on the infant gut microbiota of a low dose (ca. 25% of the RDA) of highly bioavailable iron, provided by a micronutrient powder added to a complementary food. The study aim is to determine if in-home fortification using an iron-containing micronutrient powder in Kenyan infants will improve iron status and/or modify the composition and metabolic activity of the gut microbiota. Active surveillance will be done weekly to monitor the health of the infants. Our study will be done in a subgroup (n=160) of a larger double-blind controlled feeding trial in which 330 infants will be randomized to receive a micronutrient powder containing either 2.5 mg iron or no iron for 1 year. In our substudy, the infants will be studied only over the first 6 months of the 1 year intervention. Blood samples, taken at baseline and after 6 months will be used to define the iron status and the anemia level of the infants. Stool samples (2 at baseline before intervention, 6 throughout the study and additional samples in case of diarrhea) will be obtained for analysis of the gut microbiota. In the entire study (n=330), we will measure changes in iron status over 1 year.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bacterial Infections

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
160 (Actual)

8. Arms, Groups, and Interventions

Arm Title
MixMe powder (iron & micronutrients)
Arm Type
Experimental
Arm Title
MixMe powder (micronutrients, no iron)
Arm Type
Placebo Comparator
Arm Title
Sprinkles (iron and micronutrients)
Arm Type
Experimental
Arm Description
Vitamin A 300 µg; Vitamin C 30 mg; Folic Acid 160 µg; Iron 12.5 mg; Zinc 5 mg
Arm Title
Sprinkles (micronutrients, no iron)
Arm Type
Placebo Comparator
Arm Description
Vitamin A 300 µg; Vitamin C 30 mg; Folic Acid 160 µg; Zinc 5 mg
Intervention Type
Dietary Supplement
Intervention Name(s)
fortification with iron and micronutrients
Intervention Description
Iron 0 or 2.5 mg; Copper 0.34 mg; 30 µg Iodine; 7 µg Selenium; 2.5 mg Zinc; 100 µg Vitamin A; Vitamin D 5 µg; 5 mg Tocopherol Equivalent; 30 µg Vitamin K1; 10.5 mg Thiamine; 0.5 mg Riboflavin; 0.5 mg Pyridoxine; 90 µg Folic Acid Anhydrous; 6 mg Niacinamide; 60 mg Vitamin C; 0.9 µg Vitamin B12
Intervention Type
Dietary Supplement
Intervention Name(s)
Sprinkles
Intervention Description
Daily 12.5mg Ferrous fumarate iron with microntrient is compared to no iron with micronutrients. Duration of intervention is 4 months, 80 infants will be inclulded.
Primary Outcome Measure Information:
Title
gut microbiota composition
Description
Changes in gut microbiota composition
Time Frame
Fecal sample after 2 months
Secondary Outcome Measure Information:
Title
iron status
Description
Efficacy of iron fortification in complementary foods
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
24 Weeks
Maximum Age & Unit of Time
28 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Mother at least ≥15 years of age, infants 5.5- 6.5 months Willingness to provide informed consent Apparent good health Long-term residence in study site and anticipating residing in the area for at least 3 years Speak a Mjikenda language or Kiswahili in the home Willingness to provide blood samples during clinic visits Exclusion Criteria: Hemoglobin <70 g/L for infants; these infants will be referred for treatment at the local health clinic/hospital. Acute or chronic pulmonary, cardiovascular, hepatic, renal or neurological condition or any other finding that in the opinion of the PI or co-researchers that would increase risk of participating in the study. Other conditions that in the opinion of the PI or co-researchers would jeopardize the safety or rights of a participant in the trial or would render the participant unable to comply with the protocol
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael B Zimmermann, M.D.
Organizational Affiliation
Human Nutrition Laboratory, Swiss Federal Institute of Technology
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Jane Kvalsvig, PhD
Organizational Affiliation
Department of Public Health Medicine, Nelson Mandela School of Medicine, South Africa
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kikoneni Clinic
City
Kikoneni
State/Province
Kwale district
Country
Kenya

12. IPD Sharing Statement

Citations:
PubMed Identifier
25143342
Citation
Jaeggi T, Kortman GA, Moretti D, Chassard C, Holding P, Dostal A, Boekhorst J, Timmerman HM, Swinkels DW, Tjalsma H, Njenga J, Mwangi A, Kvalsvig J, Lacroix C, Zimmermann MB. Iron fortification adversely affects the gut microbiome, increases pathogen abundance and induces intestinal inflammation in Kenyan infants. Gut. 2015 May;64(5):731-42. doi: 10.1136/gutjnl-2014-307720. Epub 2014 Aug 20.
Results Reference
derived

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Changes in Microbiota and Iron Status After Iron Fortification of Complementary Foods

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