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Community Trial of Zinc Supplementation on Preschool Child Mortality and Morbidity in Southern Nepal - Article


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Clinical Trial: Community Trial of Zinc Supplementation on Preschool Child Mortality and Morbidity in Southern Nepal

This study is currently recruiting patients.

Sponsors and Collaborators: National Institute of Child Health and Human Development (NICHD)
United States Agency for International Development
Bill and Melinda Gates Foundation
Information provided by: National Institute of Child Health and Human Development (NICHD)

Purpose

The purpose of this study is to determine whether daily supplementation of young children in Nepal with either zinc, iron-folic acid, or both can reduce mortality and morbidity. Young children in Nepal have numerous nutritional deficiencies and high rates of morbidity and mortality. Zinc and/or iron supplementation may be a cost-effective method for reducing these risks.

Condition Treatment or Intervention Phase
Nutrition
 Drug: zinc sulphate dietary supplement
 Drug: iron sulphate-folic acid dietary supplement
Phase III

MedlinePlus consumer health information 

Study Type: Interventional
Study Design: Prevention, Randomized, Double-Blind, Placebo Control, Factorial Assignment, Efficacy Study

Official Title: Zinc Supplementation Impact on Child Mortality--Nepal

Further Study Details: 
Primary Outcomes: Death among children 1-36 months of age
Secondary Outcomes: Incidence rates of selected morbidities including diarrhea, dysentery, acute respiratory infections
Expected Total Enrollment:  58000

Study start: October 2001;  Expected completion: December 2006
Last follow-up: December 2005;  Data entry closure: March 2006

Mortality rates among preschool age children in Nepal and many other developing countries remain high despite significant progress made over the past 20 years. There remain significant nutritional deficiencies in these populations, especially important are vitamin and mineral deficiencies.

Comparisons: In this study, we are comparing the morbidity and mortality experience for children 1-36 months of age randomized to one of four daily supplementation regimens: placebo, zinc alone, iron-folic acid alone, zinc + iron-folic acid.

Eligibility

Ages Eligible for Study:  1 Month   -   36 Months,  Genders Eligible for Study:  Both

Accepts Healthy Volunteers

Criteria

Inclusion Criteria:

  • All children 1-35 months of age living in 30 Village Development Committees of Sarlahi District in southern Nepal.

Exclusion Criteria:

  • Parent refusal

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00109551

James M Tielsch, PhD      410 955-2436    jtielsch@jhsph.edu

Maryland
      Johns Hopkins Bloomberg School of Public Health, Baltimore,  Maryland,  21205-2103,  United States; Completed

New York
      Cornell University Division of Nutritional Sciences, Ithaca,  New York,  14853,  United States; Completed

Nepal
      Nepal Nutrition Intervention Project-Sarlahi, Kathmandu and Sarlahi District,  Nepal; Recruiting
Subarna K Khatry, MBBS  977 1-4261829    skk@mos.com.np 
Steven C LeClerq, MPH  977 1-4261829    sleclerq@mos.com.np 
Subarna K Khatry, MBBS,  Sub-Investigator
Steven C LeClerq, MPH,  Sub-Investigator
Ramesh Adhikari, MD,  Sub-Investigator

Study chairs or principal investigators

James M Tielsch, PhD,  Principal Investigator,  Johns Hopkins Bloomberg School of Public Health   

More Information

Study ID Numbers:  R01 HD38753; R01-HD38753
Record last reviewed:  April 2005
Last Updated:  April 29, 2005
Record first received:  April 28, 2005
ClinicalTrials.gov Identifier:  NCT00109551
Health Authority: United States: Federal Government; Nepal: Nepal Health Research Council (Awaiting confirmation)
ClinicalTrials.gov processed this record on 2005-05-03


Source: ClinicalTrials.gov
Cache Date: May 4, 2005


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Page Updated: June 1, 2005
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