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Efficacy of Iron Fortified Complementary Food and IPT of Malaria in Young Children in Côte d'Ivoire

Primary Purpose

Anemia

Status
Completed
Phase
Not Applicable
Locations
Côte D'Ivoire
Study Type
Interventional
Intervention
SP/amodiaquine
FeFum fortified porridge
SP/Amodiaquine + FeFum fortified porridge
Ferric pyrophosphate fortified porridge
Placebo
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 Anemia focused on measuring anemia, malaria, malnutrition, iron fortification, intermittent preventive treatment, subsaharan africa, ivory coast, young children

Eligibility Criteria

12 Months - 36 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Children, aged 12 - 36 months, both sexes
  • Absence of major systemic illnesses (as assessed by medical doctor upon initial full clinical assessment)
  • Registered in DSS Taabo and anticipated residence in the study area for at least 1 year
  • No severe anaemia, i.e. Hb ≥70 g/L in infants, as assessed by a Coulter Counter device
  • No known or reported hypersensitivity to sulfadoxine-pyrimethamine, amodiaquine
  • No known or reported history of significant chronic illness
  • Written informed consent of parents or legal guardian

Exclusion Criteria:

  • severe anaemia, i.e. Hb ≥70 g/L in infants, as assessed by a Coulter Counter device
  • major systemic illnesses (as assessed by medical doctor upon initial full clinical assessment)
  • known or reported hypersensitivity to albendazole, sulfadoxine-pyrimethamine, amodiaquine
  • known or reported history of significant chronic illness

Sites / Locations

  • Hopital General de Taabo Cite

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm Type

Placebo Comparator

Experimental

Experimental

Experimental

Experimental

Arm Label

Placebo

FeFum porridge + IPT of malaria

IPT of malaria

FeFum porridge

FePP porridge

Arm Description

Placebo

Outcomes

Primary Outcome Measures

Hemoglobin
The study population will consist of 12 to 36-month-old infants in villages covered by the Taabo DSS site. Assuming a mean Hb of 97.3±19.6 g/l and that an increase of 8 g/l in Hb would be clinically relevant, and allowing for a dropout rate of 20%, we calculated that 125 infants per group were initially needed to achieve a power level of 90% at a 5% level of significance.

Secondary Outcome Measures

Iron status indicators (SF, TfR)
The study population will consist of 12 to 36-month-old infants in villages covered by the Taabo DSS site.
Malaria prevalence
The study population will consist of 12 to 36-month-old infants in villages covered by the Taabo DSS site.

Full Information

First Posted
July 3, 2012
Last Updated
September 23, 2013
Sponsor
Swiss Federal Institute of Technology
Collaborators
Swiss Tropical & Public Health Institute, Swiss National Science Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT01634945
Brief Title
Efficacy of Iron Fortified Complementary Food and IPT of Malaria in Young Children in Côte d'Ivoire
Official Title
Aetiology, Prevention and Control of Anaemia in Sub-Saharan Africa - Work Package 2: Efficacy Study: Efficacy of 2 Iron Fortified Porridges and IPT for the Prevention of Anemia in Young Children in Côte d'Ivoire.
Study Type
Interventional

2. Study Status

Record Verification Date
September 2013
Overall Recruitment Status
Completed
Study Start Date
April 2012 (undefined)
Primary Completion Date
May 2013 (Actual)
Study Completion Date
May 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Swiss Federal Institute of Technology
Collaborators
Swiss Tropical & Public Health Institute, Swiss National Science Foundation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The proposed project is aimed at testing two interventions, namely a highly bioavailable iron compound and a combination of SP plus amodiaquine for intermittent preventive treatment (IPT) of malaria, to reduce anaemia in very young children.
Detailed Description
Efficacy study - ANAEMIA project Côte d'Ivoire The proposed project is aimed at testing two interventions, namely a highly bioavailable iron compound and a combination of SP plus amodiaquine for intermittent preventive treatment (IPT) of malaria, to reduce anaemia in very young children. The fortified product will be provided as porridge (Nutribon produced by PKL) with an optimized formula (2 mg in the form of NaFeEDTA and 3.8 mg in the form of ferrous fumarate) of the premix. In addition, we will assess the Nutribon product currently available on the market and we will compare it to an optimized premix formula. The current and the optimized formula contain each 2 mg iron in the form of NaFeEDTA. In addition to the NaFeEDTA the current premix contains 3.8 mg in the form of ferric pyrophosphate, which is less bioavailable than the 3.8 mg ferrous fumarate in the optimized formula. The study will be carried out between May and December 2012 which includes the rainy season (April - October) with its two peaks in Côte d'Ivoire and thus the period when malaria transmission is highest. The study will be implemented in a Health and Demographic Surveillance System in Taabo in Côte d'Ivoire and comprise 625 children between 12 to 36 months. 375 eligible infants will receive a fortified porridge (250 with the improved formula and 125 with the current formula), whereas 250 infants will continue with their local diet (control group). Infants receiving the optimized formula and infants in the control group will be randomly assigned to IPT of malaria (125 in each group) or placebo (125 in each group). Thus, infants can be assigned to one of the following five groups: 1. group (n=125): fortified porridge (optimized formula) and IPT of malaria 2. group (n=125): fortified porridge (optimized formula) and placebo 3. group (n=125): local diet and IPT of malaria and 4. group (n=125): local diet and placebo. 5. group (n=125): fortified porridge (current formula) and placebo, representing the current situation in Côte d'Ivoire in infants consuming fortified complementary food. This efficacy trial will deepen our understanding in preventing anaemia and the interaction of bioavailable iron compounds with an antimalarial drug and related conditions in very young children. Further, the study should demonstrate whether the earlier study failed to show an impact on anaemia due to the use of an iron compound that lacked bioavailability and/or using an antimalarial drug in the IPT intervention arm that lacked efficacy perhaps due to resistance by P. falciparum, or other yet to be investigated causes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anemia
Keywords
anemia, malaria, malnutrition, iron fortification, intermittent preventive treatment, subsaharan africa, ivory coast, young children

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
629 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo
Arm Title
FeFum porridge + IPT of malaria
Arm Type
Experimental
Arm Title
IPT of malaria
Arm Type
Experimental
Arm Title
FeFum porridge
Arm Type
Experimental
Arm Title
FePP porridge
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
SP/amodiaquine
Intervention Description
One dose of SP (500 mg sulfadoxine plus 25 mg pyrimethamine, or half of the dose if body weight =< 10 kg) and three daily doses of Amodiaquine (1. Day: 200 mg, 2. Day: 200 mg and 3. Day: 100 mg, or half of the dose each day if body weight =< 10 kg), every three months, i.e. 3 times during 9 consecutive months.
Intervention Type
Dietary Supplement
Intervention Name(s)
FeFum fortified porridge
Intervention Description
6 times per week supply of iron fortified porridge (25 g portion containing 5.8 mg of iron: 2 mg as NaFeEDTA + 3.8 mg as ferrous fumarate) for 9 months.
Intervention Type
Drug
Intervention Name(s)
SP/Amodiaquine + FeFum fortified porridge
Intervention Description
One dose of SP (500 mg sulfadoxine plus 25 mg pyrimethamine, or half of the dose if body weight =< 10 kg) and three daily doses of Amodiaquine (1. Day: 200 mg, 2. Day: 200 mg and 3. Day: 100 mg, or half of the dose each day if body weight =< 10 kg), every three months, i.e. 3 times during 9 consecutive months. 6 times per week supply of iron fortified porridge (25 g portion containing 5.8 mg of iron: 2 mg as NaFeEDTA + 3.8 mg as ferrous fumarate) for 9 months.
Intervention Type
Dietary Supplement
Intervention Name(s)
Ferric pyrophosphate fortified porridge
Intervention Description
6 days per week supply of iron fortified porridge (25 g portion containing 5.8 mg of iron: 2 mg as NaFeEDTA + 3.8 mg as ferric pyrophosphate) for 9 months.
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Placebo of SP/Amodiaquine every 3 months for 9 months. No dietary intervention.
Primary Outcome Measure Information:
Title
Hemoglobin
Description
The study population will consist of 12 to 36-month-old infants in villages covered by the Taabo DSS site. Assuming a mean Hb of 97.3±19.6 g/l and that an increase of 8 g/l in Hb would be clinically relevant, and allowing for a dropout rate of 20%, we calculated that 125 infants per group were initially needed to achieve a power level of 90% at a 5% level of significance.
Time Frame
9 months
Secondary Outcome Measure Information:
Title
Iron status indicators (SF, TfR)
Description
The study population will consist of 12 to 36-month-old infants in villages covered by the Taabo DSS site.
Time Frame
9 months
Title
Malaria prevalence
Description
The study population will consist of 12 to 36-month-old infants in villages covered by the Taabo DSS site.
Time Frame
9 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Months
Maximum Age & Unit of Time
36 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children, aged 12 - 36 months, both sexes Absence of major systemic illnesses (as assessed by medical doctor upon initial full clinical assessment) Registered in DSS Taabo and anticipated residence in the study area for at least 1 year No severe anaemia, i.e. Hb ≥70 g/L in infants, as assessed by a Coulter Counter device No known or reported hypersensitivity to sulfadoxine-pyrimethamine, amodiaquine No known or reported history of significant chronic illness Written informed consent of parents or legal guardian Exclusion Criteria: severe anaemia, i.e. Hb ≥70 g/L in infants, as assessed by a Coulter Counter device major systemic illnesses (as assessed by medical doctor upon initial full clinical assessment) known or reported hypersensitivity to albendazole, sulfadoxine-pyrimethamine, amodiaquine known or reported history of significant chronic illness
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rita Wegmüller, Doctor
Organizational Affiliation
Swiss Federal Institute of Technology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hopital General de Taabo Cite
City
Taabo Cite
Country
Côte D'Ivoire

12. IPD Sharing Statement

Citations:
PubMed Identifier
28708072
Citation
Glinz D, Wegmuller R, Ouattara M, Diakite VG, Aaron GJ, Hofer L, Zimmermann MB, Adiossan LG, Utzinger J, N'Goran EK, Hurrell RF. Iron Fortified Complementary Foods Containing a Mixture of Sodium Iron EDTA with Either Ferrous Fumarate or Ferric Pyrophosphate Reduce Iron Deficiency Anemia in 12- to 36-Month-Old Children in a Malaria Endemic Setting: A Secondary Analysis of a Cluster-Randomized Controlled Trial. Nutrients. 2017 Jul 14;9(7):759. doi: 10.3390/nu9070759.
Results Reference
derived
PubMed Identifier
26377199
Citation
Glinz D, Hurrell RF, Ouattara M, Zimmermann MB, Brittenham GM, Adiossan LG, Righetti AA, Seifert B, Diakite VG, Utzinger J, N'Goran EK, Wegmuller R. The effect of iron-fortified complementary food and intermittent preventive treatment of malaria on anaemia in 12- to 36-month-old children: a cluster-randomised controlled trial. Malar J. 2015 Sep 17;14:347. doi: 10.1186/s12936-015-0872-3.
Results Reference
derived

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Efficacy of Iron Fortified Complementary Food and IPT of Malaria in Young Children in Côte d'Ivoire

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