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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02253095
Other study ID # EE-zinc-alb-micronut
Secondary ID
Status Completed
Phase N/A
First received September 26, 2014
Last updated June 2, 2015
Start date October 2014
Est. completion date April 2015

Study information

Verified date June 2015
Source Washington University School of Medicine
Contact n/a
Is FDA regulated No
Health authority Malawi: College of Medicine Research and Ethics Committee
Study type Interventional

Clinical Trial Summary

Randomized, double-blind, placebo controlled trial of a combined intervention of zinc, albendazole, and multiple micronutrients in improving environmental enteropathy in Malawian children.


Recruitment information / eligibility

Status Completed
Enrollment 253
Est. completion date April 2015
Est. primary completion date April 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 12 Months to 35 Months
Eligibility Inclusion Criteria:

- children residing in catchment area of Limela, Machinga District, Malawi

- aged 12-35 months

- youngest eligible child in each household

Exclusion Criteria:

- severe 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

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Albendazole

Dietary Supplement:
Zinc

Multiple Micronutrient Supplement

Drug:
Placebo


Locations

Country Name City State
Malawi Limela Rural Site Limela Machinga Distric

Sponsors (2)

Lead Sponsor Collaborator
Washington University School of Medicine University of Malawi

Country where clinical trial is conducted

Malawi, 

Outcome

Type Measure Description Time frame Safety issue
Primary Dual Sugar Absorption Test lactulose-mannitol ratio in urine 12 weeks No
Primary Dual Sugar Absorption Test lactulose-mannitol ratio in urine 24 weeks No
Secondary Lactulose Excretion percentage of ingested lactulose excreted in urine 12 weeks No
Secondary Lactulose Excretion percentage of ingested lactulose excreted in urine 24 weeks No
Secondary Mannitol Excretion percentage of ingested mannitol excreted in urine 12 weeks No
Secondary Mannitol Excretion percentage of ingested mannitol excreted in urine 24 weeks No
See also
  Status Clinical Trial Phase
Completed NCT01832636 - Intervention and Mechanisms of Alanyl-Glutamine for Inflammation, Nutrition, and Enteropathy Phase 3
Active, not recruiting NCT04565821 - Feasibility Study to Assess a Trans-nasal Intestinal Potential Difference Probe N/A
Completed NCT01593033 - Effectiveness of Micronutrient Supplementation and Fish Oil + Micronutrient Supplementation in the Treatment of Environmental Enteropathy N/A
Active, not recruiting NCT03713502 - Enteropathy and Diabetes in HIV Patients
Not yet recruiting NCT05608928 - Ability of the Probiotic Vivomixx to Improve Environmental Enteropathy in Pregnant Women: a Proof of Concept Trial in Bangladesh, Pakistan, Senegal and Zambia Phase 2
Completed NCT02472301 - The Impact of Legumes vs Corn-soy Flour on Environmental Enteric Dysfunction in Rural Malawian Children 1-3 Year Olds N/A