Marasmus Clinical Trial
Official title:
Effectiveness of Safe Drinking Water in Community Based Treatment of Severe Acute Malnutrition
Verified date | January 2017 |
Source | Action Contre la Faim |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study builds evidence on the importance of using safe drinking water during the nutritional treatment of children affected by Severe Acute Malnutrition (SAM). The following hypotheses will be tested: 1.The addition of safe drinking water to SAM treatment will reduce exposure to pathogens that cause diarrhoeal disease, thereby reducing diarrhoea incidence among enrolled children. 2.Reductions in pathogen exposure and diarrhoeal disease will result in shorter recovery pe-riods for children with SAM. The study will evaluate the effectiveness of safe drinking water in reducing SAM treatment cost and duration and will provide recommendations for improving SAM treatment protocols.
Status | Active, not recruiting |
Enrollment | 820 |
Est. completion date | March 2017 |
Est. primary completion date | October 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 6 Months to 59 Months |
Eligibility |
Inclusion Criteria: - Children in each selected community will be eligible for inclusion in the study if they are 1. between six and 59 months of age, 2. diagnosed as an uncomplicated SAM case 3. enrolled in ACF's CMAMprogram 4. if the child's caretaker gives consent for the child's participation. Exclusion Criteria: - Children will be ineligible for participation if 1. they have a diagnosis of kwashiorkor; OR 2) they require in-patient treatment for SAM 2. their caretakers are unwilling or unable to agree to their participation. - Children graduating from in-patient treatment (i.e no remaining medical complications) to the out-patient CMAM program will be eligible for participation. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Action Contre la Faim | Johns Hopkins University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Recovery rate | the total number of cured children / total number of exited children (including cured, deceased, and lost to follow-up) | 5 months |
Status | Clinical Trial | Phase | |
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