Water-based Zinc Intervention Trial in Zinc Deficient Children
Primary Purpose
Zinc Deficiency, Diarrhea
Status
Terminated
Phase
Early Phase 1
Locations
Benin
Study Type
Interventional
Intervention
zinc enriching filter (LifeStrawFamily)
placebo filter
disinfection tablets
Sponsored by
About this trial
This is an interventional treatment trial for Zinc Deficiency
Eligibility Criteria
Inclusion Criteria:
- 2-5 year old children
- subjects residing in the study area for the whole study period
Exclusion Criteria:
- subject with severe anemia (Hb < 7 g/dl)
- subjects affected by chronic medical illnesses known to interact with zinc metabolism
- subjects receiving zinc supplementation or other medicines that may affect zinc metabolism
Sites / Locations
- Hopital de Zone
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Placebo Comparator
Active Comparator
Arm Label
intervention filter
placebo filter
disinfection tablets
Arm Description
children consuming purified and zinc enriched water delivered by a household-based water filter
children consuming purified water delivered by a household-based water filter
children will consume water treated with government promoted disinfection tablets (aquatabs)
Outcomes
Primary Outcome Measures
Zinc status
At baseline, endpoint and at a randomly assigned screening between month 1 and 11, a 6 ml whole blood sample will be collected by venipuncture in 2-5y children (N=270). The blood sample will be used to determine concentration of zinc in the serum (SZn). Inflammation indicator C-reactive protein (CRP) will be analysed to adjust SZn values.
Secondary Outcome Measures
Gut microbiota characterisation
At baseline and month 2, stool samples will be collected in 60 children (20 per study arm) for gut flora characterisation.
Iron status
At baseline, endpoint and at a randomly assigned screening between month 1 and 11, a 6 ml whole blood sample will be collected by venipuncture in 2-5y children (N=270). The blood sample will be used to determine the levels of haemoglobin (Hb) and serum ferritin (SF) for the assessment of iron status.
Growth rate
At baseline, midpoint and endpoint weight, height and MUAC will be measured in 2-5y children (N=270). Anthropometric measurements will be used to determine growth rate.
Diarrhea prevalence
Study children will be weekly surveyed for diarrhea occurrence. Mothers/tutors will be requested to report any diarrhea episode occurred in the last 48 hours.
Full Information
NCT ID
NCT01472211
First Posted
November 9, 2011
Last Updated
June 17, 2013
Sponsor
Swiss Federal Institute of Technology
Collaborators
Université d'Abomey-Calavi
1. Study Identification
Unique Protocol Identification Number
NCT01472211
Brief Title
Water-based Zinc Intervention Trial in Zinc Deficient Children
Official Title
An Efficacy Trial of a Gravity-fed Household Water Treatment Device as a Delivery System for Zinc in Zinc Deficient Preschool Children and Pregnant Women From Rural Settings With Poor Access to Potable Water in Benin.
Study Type
Interventional
2. Study Status
Record Verification Date
June 2013
Overall Recruitment Status
Terminated
Why Stopped
Zn released from vehicle led to fortification levels higher than planned. New filter will be developed.
Study Start Date
September 2011 (undefined)
Primary Completion Date
December 2011 (Actual)
Study Completion Date
September 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Swiss Federal Institute of Technology
Collaborators
Université d'Abomey-Calavi
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The overall aim of this trial is to determine whether the use of the household-based water treatment device Life Straw Family (LSF) can be an effective strategy to improve zinc status and health status of vulnerable populations in developing country rural settings with poor access to potable water.
To assess the effectiveness of the LSF strategy (a filter delivering purified and zinc enriched water) a double blind controlled field efficacy trial will take place over a period of 12 months in rural villages in the district of Natitingou, North-West Benin. In order to attain the research objectives the efficacy trial will envisage 3 arms: intervention (zinc enriching filter), placebo (filter) and control group (disinfection tables). During the trial the following outcomes will be monitored: zinc status and growth rate of the participating children, zinc status and pregnancy outcome in a sub-sample of pregnant women (pregnancy sub-study), diarrhea prevalence in all participating subjects, water quality, zinc enrichment of water, and modality and consistency of use of the LSF-device by the study population.
The study hypotheses are: 1) the use of the LSF-device will reduce microbiological contamination of the household water, 2) the use of the LSF-device will increase zinc intakes and serum zinc concentration in preschool children, 3) the use of the LSF-device will increase zinc intakes and serum zinc concentration in pregnant women, 4) the achievement of 1 and 2 will improve growth and lower frequency and length of diarrhea episodes in participating preschool children, 5) the achievement of 1 and 3 will improve pregnancy outcome and lower frequency and length of diarrhea episodes in participating pregnant women, 6) the use of the LSF-device will lower frequency and length of diarrhea episodes in participating households members.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Zinc Deficiency, Diarrhea
7. Study Design
Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
317 (Actual)
8. Arms, Groups, and Interventions
Arm Title
intervention filter
Arm Type
Experimental
Arm Description
children consuming purified and zinc enriched water delivered by a household-based water filter
Arm Title
placebo filter
Arm Type
Placebo Comparator
Arm Description
children consuming purified water delivered by a household-based water filter
Arm Title
disinfection tablets
Arm Type
Active Comparator
Arm Description
children will consume water treated with government promoted disinfection tablets (aquatabs)
Intervention Type
Device
Intervention Name(s)
zinc enriching filter (LifeStrawFamily)
Other Intervention Name(s)
LifeStrawFamily by Vestergaards-Frandsen (Switzerland)
Intervention Description
filter purifies water and enriches it with zinc at 1-4 mg/l.
Intervention Type
Device
Intervention Name(s)
placebo filter
Other Intervention Name(s)
LifeStrawFamily by Vestergaards-Frandsen (Switzerland)
Intervention Description
filter purifies water
Intervention Type
Other
Intervention Name(s)
disinfection tablets
Other Intervention Name(s)
Aquatabs water purification tablets
Intervention Description
government promoted tablets disinfect water
Primary Outcome Measure Information:
Title
Zinc status
Description
At baseline, endpoint and at a randomly assigned screening between month 1 and 11, a 6 ml whole blood sample will be collected by venipuncture in 2-5y children (N=270). The blood sample will be used to determine concentration of zinc in the serum (SZn). Inflammation indicator C-reactive protein (CRP) will be analysed to adjust SZn values.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Gut microbiota characterisation
Description
At baseline and month 2, stool samples will be collected in 60 children (20 per study arm) for gut flora characterisation.
Time Frame
2 months
Title
Iron status
Description
At baseline, endpoint and at a randomly assigned screening between month 1 and 11, a 6 ml whole blood sample will be collected by venipuncture in 2-5y children (N=270). The blood sample will be used to determine the levels of haemoglobin (Hb) and serum ferritin (SF) for the assessment of iron status.
Time Frame
12 months
Title
Growth rate
Description
At baseline, midpoint and endpoint weight, height and MUAC will be measured in 2-5y children (N=270). Anthropometric measurements will be used to determine growth rate.
Time Frame
12 months
Title
Diarrhea prevalence
Description
Study children will be weekly surveyed for diarrhea occurrence. Mothers/tutors will be requested to report any diarrhea episode occurred in the last 48 hours.
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
2-5 year old children
subjects residing in the study area for the whole study period
Exclusion Criteria:
subject with severe anemia (Hb < 7 g/dl)
subjects affected by chronic medical illnesses known to interact with zinc metabolism
subjects receiving zinc supplementation or other medicines that may affect zinc metabolism
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael Zimmermann, Prof. Dr.med.
Organizational Affiliation
Swiss Federal Institute of Technology
Official's Role
Study Chair
Facility Information:
Facility Name
Hopital de Zone
City
Natitingou
State/Province
Atacora
Country
Benin
12. IPD Sharing Statement
Citations:
PubMed Identifier
26609168
Citation
Galetti V, Mitchikpe CE, Kujinga P, Tossou F, Hounhouigan DJ, Zimmermann MB, Moretti D. Rural Beninese Children Are at Risk of Zinc Deficiency According to Stunting Prevalence and Plasma Zinc Concentration but Not Dietary Zinc Intakes. J Nutr. 2016 Jan;146(1):114-23. doi: 10.3945/jn.115.216606. Epub 2015 Nov 25.
Results Reference
derived
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Water-based Zinc Intervention Trial in Zinc Deficient Children
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