Delivery of Iron and Zinc Supplements: Evaluation of Interaction Effect on Biochemical and Clinical Outcomes
Primary Purpose
Anemia, Diarrhea, Iron
Status
Completed
Phase
Phase 4
Locations
Bangladesh
Study Type
Interventional
Intervention
iron and zinc combined
iron and zinc on separate days
iron
Zinc
placebo
Sponsored by
About this trial
This is an interventional prevention trial for Anemia focused on measuring zinc, iron, interaction, diarrhea, delivery
Eligibility Criteria
Inclusion Criteria:
- Children 6-18 months old
- Permanent residents of the selected villages
Exclusion Criteria:
- Severe malnutrition requiring hospitalization (defined as weight for height <-3 SD Z-score)
- Severe anemia requiring treatment (hemoglobin < 70 g/L)
- Chronic illness that would impair feeding ability
- Likely to move in next 6 months.
- Fever greater than 38.5
- Regular iron supplementation
Sites / Locations
- ICDDR,B
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Arm Type
Experimental
Experimental
Experimental
Experimental
Placebo Comparator
Arm Label
combined iron and zinc
Separate iron and zinc
iron alone
zinc alone
placebo
Arm Description
Iron and zinc together
Iron and zinc on separate days
Iron
Zinc
Outcomes
Primary Outcome Measures
Incidence of Diarrhea
A diarrhea episode was defined as three or more loose, liquid, or watery stools for 2 consecutive days, separated in time from an earlier or subsequent episode by at least 2 consecutive diarrhea-free days.
Secondary Outcome Measures
Change in Hemoglobin
Change in Zinc Status
Percent Anemic
Full Information
NCT ID
NCT00470158
First Posted
May 3, 2007
Last Updated
April 18, 2018
Sponsor
Johns Hopkins Bloomberg School of Public Health
Collaborators
International Centre for Diarrhoeal Disease Research, Bangladesh, United States Agency for International Development (USAID), Agency for Healthcare Research and Quality (AHRQ)
1. Study Identification
Unique Protocol Identification Number
NCT00470158
Brief Title
Delivery of Iron and Zinc Supplements: Evaluation of Interaction Effect on Biochemical and Clinical Outcomes
Official Title
Delivery of Iron and Zinc Supplements: Evaluation of Interaction Effect on Biochemical and Clinical Outcomes
Study Type
Interventional
2. Study Status
Record Verification Date
December 2009
Overall Recruitment Status
Completed
Study Start Date
May 2007 (undefined)
Primary Completion Date
February 2008 (Actual)
Study Completion Date
February 2008 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins Bloomberg School of Public Health
Collaborators
International Centre for Diarrhoeal Disease Research, Bangladesh, United States Agency for International Development (USAID), Agency for Healthcare Research and Quality (AHRQ)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
With the long-term public health goal of developing an effective micronutrient supplementation program to improve child health by improving iron and zinc status and decreasing morbidity due to diarrhea in areas with high rates of childhood malnutrition, we seek to determine the most efficacious method of decreasing childhood morbidity and mortality due to diarrhea in toddlers by re-examining the issue of iron and zinc interaction and determining if this interaction can be minimized by separate administration of iron and zinc supplementation.
Detailed Description
Iron supplementation is used in reducing anemia and improving hemoglobin status. Zinc supplementation is emerging as possibly an efficacious preventive measure in decreasing incidence of severe diarrhea. Previous studies have suggested interactions of zinc and iron when given together, reducing the effects of supplementation with both minerals. One study in Peru has shown a decrease in interaction effect with separate supplementation of iron and zinc in time when compared to iron administration alone or placebo; however, an evaluation of clinical outcomes and zinc or iron status when iron and zinc are administered separately compared to supplementation of zinc and iron together or each alone has not previously been done. This trial will assess the effect of iron and zinc supplementation given on alternate days compared with giving them together in a combined supplement.
We propose a randomized, double blind, placebo-controlled community trial of children 6-23 months in Mirzapur, Bangladesh. We will recruit and enroll 1000 children 6-23 months old who are permanent residents of the selected villages. Each child will be randomly assigned to 1) daily alternating zinc and placebo 2) daily alternating iron/folic acid and placebo 3) daily alternating zinc/iron/folic acid and placebo 4) daily alternating zinc and iron/folic acid 5) daily placebo. Primary outcomes will include incidence of severe diarrhea, evaluated weekly for 6 months, hemoglobin, prevalence of anemia, and serum zinc.
Analysis of the data will be done to compare the effect of separate iron and zinc supplementation as compared to combined iron and zinc supplementation as well as compared to iron, zinc, or placebo single supplementation. We will evaluate the difference in incidence rate of severe diarrhea, serum hemoglobin, percent anemia, and serum zinc. Since this will be a randomized, double-blind, placebo controlled trial, differences in effect will be most likely explained by the timing of supplement doses. If there is an improvement in clinical and biochemical outcomes, this would be consistent with a decreased interaction of absorption. If no difference is found, there may be another mechanism for the seeming interaction of iron and zinc besides that of mutually inhibitory absorption in the intestine.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anemia, Diarrhea, Iron
Keywords
zinc, iron, interaction, diarrhea, delivery
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
1000 (Actual)
8. Arms, Groups, and Interventions
Arm Title
combined iron and zinc
Arm Type
Experimental
Arm Description
Iron and zinc together
Arm Title
Separate iron and zinc
Arm Type
Experimental
Arm Description
Iron and zinc on separate days
Arm Title
iron alone
Arm Type
Experimental
Arm Description
Iron
Arm Title
zinc alone
Arm Type
Experimental
Arm Description
Zinc
Arm Title
placebo
Arm Type
Placebo Comparator
Intervention Type
Dietary Supplement
Intervention Name(s)
iron and zinc combined
Other Intervention Name(s)
Tablets were manufactured by Nutriset, S.A.S. (Malaunay, France).
Intervention Description
Children >= 12 months received an average of 5mg zinc/day, 6.25 Iron/day, and 25IU folic acid/day. children<12 received half that dose. This dose was alternated daily with placebo. Dissolvable doses were distributed in blister packs and reconstituted with a teaspoon of water. Doses were administered in the morning. For missed doses, the mother gave the child the next morning dose, and a second dose in the evening.
Intervention Type
Dietary Supplement
Intervention Name(s)
iron and zinc on separate days
Other Intervention Name(s)
Tablets were manufactured by Nutriset, S.A.S. (Malaunay, France).
Intervention Description
Children >= 12 months received an average of 5mg zinc/day, alternating daily with 6.25 Iron/day, and 25IU folic acid/day. Children<12 received half that dose. Dissolvable doses were distributed in blister packs and reconstituted with a teaspoon of water. Doses were administered in the morning. For missed doses, the mother gave the child the next morning dose, and a second dose in the evening.
Intervention Type
Dietary Supplement
Intervention Name(s)
iron
Intervention Description
Children >= 12 months received an average 6.25 Iron/day, and 25IU folic acid/day. Children<12 received half that dose. This dose was alternated daily with placebo. Dissolvable doses were distributed in blister packs and reconstituted with a teaspoon of water. Doses were administered in the morning. For missed doses, the mother gave the child the next morning dose, and a second dose in the evening.
Intervention Type
Dietary Supplement
Intervention Name(s)
Zinc
Intervention Description
Children >= 12 months received an average of 5mg zinc/day. Children<12 received half that dose. This dose was alternated daily with placebo. Dissolvable doses were distributed in blister packs and reconstituted with a teaspoon of water. Doses were administered in the morning. For missed doses, the mother gave the child the next morning dose, and a second dose in the evening.
Intervention Type
Dietary Supplement
Intervention Name(s)
placebo
Intervention Description
Children received daily placebo. Dissolvable doses were distributed in blister packs and reconstituted with a teaspoon of water. Doses were administered in the morning. For missed doses, the mother gave the child the next morning dose, and a second dose in the evening.
Primary Outcome Measure Information:
Title
Incidence of Diarrhea
Description
A diarrhea episode was defined as three or more loose, liquid, or watery stools for 2 consecutive days, separated in time from an earlier or subsequent episode by at least 2 consecutive diarrhea-free days.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Change in Hemoglobin
Time Frame
6 months
Title
Change in Zinc Status
Time Frame
6 months
Title
Percent Anemic
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
18 Months
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Children 6-18 months old
Permanent residents of the selected villages
Exclusion Criteria:
Severe malnutrition requiring hospitalization (defined as weight for height <-3 SD Z-score)
Severe anemia requiring treatment (hemoglobin < 70 g/L)
Chronic illness that would impair feeding ability
Likely to move in next 6 months.
Fever greater than 38.5
Regular iron supplementation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert E Black, MD, MPH
Organizational Affiliation
Johns Hopkins Bloomberg School of Public Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
ICDDR,B
City
Dhaka
State/Province
Mohakhali
ZIP/Postal Code
1212
Country
Bangladesh
12. IPD Sharing Statement
Citations:
PubMed Identifier
19904293
Citation
Chang S, El Arifeen S, Bari S, Wahed MA, Rahman KM, Rahman MT, Mahmud AB, Begum N, Zaman K, Baqui AH, Black RE. Supplementing iron and zinc: double blind, randomized evaluation of separate or combined delivery. Eur J Clin Nutr. 2010 Feb;64(2):153-60. doi: 10.1038/ejcn.2009.127. Epub 2009 Nov 11.
Results Reference
result
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Delivery of Iron and Zinc Supplements: Evaluation of Interaction Effect on Biochemical and Clinical Outcomes
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