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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01828814
Other study ID # Epicentre
Secondary ID
Status Completed
Phase N/A
First received March 4, 2013
Last updated April 27, 2017
Start date July 2011
Est. completion date October 2012

Study information

Verified date April 2017
Source Epicentre
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Options for large-scale preventive distributions include fortified blended flours, ready-to-use foods and direct cash transfer either alone or in combination with family protective rations. Finding the most appropriate strategy is essential to prevent child malnutrition in countries like Niger with annual hunger gaps. Here, the investigators compare different preventive strategies on the incidence of acute malnutrition among children 6 to 23 months.


Recruitment information / eligibility

Status Completed
Enrollment 7836
Est. completion date October 2012
Est. primary completion date October 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 6 Months to 24 Months
Eligibility Inclusion Criteria:

- resident in selected villages

- height between 60 and 80 cm.

Exclusion Criteria:

- refusal to participate

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Niger Villages Madarounfa Maradi

Sponsors (2)

Lead Sponsor Collaborator
Epicentre United Nations World Food Programme (WFP)

Country where clinical trial is conducted

Niger, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of severe acute malnutrition Severe acute malnutrition was defined as : Weight for Height Z-score (WHO Standards 2006)< -3 and/or mid-upper arm circumference (MUAC) < 115mm and/or bipedal oedema. MUAC was measured at the midpoint of a child's left arm with a plastic measuring tape with a precision of 1 mm.
These indicators were evaluated monthly during the entire follow-up (15 months).
15 months
Secondary Mortality Mortality events include all reports for which the cause for absence from surveillance visits was reported to be death by a family member. duration of follow-up (15 months)
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