Environmental Enteric Dysfunction Clinical Trial
Verified date | May 2018 |
Source | Washington University School of Medicine |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Randomized, double-blind, placebo controlled trial of daily lactoferrin and lysozyme supplementation in improving environmental enteric dysfunction in Malawian children
Status | Completed |
Enrollment | 235 |
Est. completion date | December 2017 |
Est. primary completion date | December 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 12 Months to 35 Months |
Eligibility |
Inclusion Criteria: - children aged 12-35 months - youngest eligible child in each household Exclusion Criteria: - severe or moderate acute malnutrition - severe chronic illness - children unable to drink 20 mL of dual sugar solution - children in need of acute medical treatment for illness or injury at time of enrollment |
Country | Name | City | State |
---|---|---|---|
Malawi | Malawi | Blantyre |
Lead Sponsor | Collaborator |
---|---|
Washington University School of Medicine | University of Malawi |
Malawi,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Linear Growth | changes in linear growth | 16 weeks | |
Primary | Dual Sugar Absorption Test | lactulose-mannitol ratio in urine | 8 weeks | |
Primary | Dual Sugar Absorption Test | lactulose-mannitol ratio in urine | 16 weeks | |
Secondary | Lactulose Excretion | percentage of ingested lactulose excreted in urine | 8 weeks | |
Secondary | Lactulose Excretion | percentage of ingested lactulose excreted in urine | 16 weeks | |
Secondary | Mannitol Excretion | percentage of ingested mannitol excreted in urine | 8 weeks | |
Secondary | Mannitol Excretion | percentage of ingested mannitol excreted in urine | 16 weeks |
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