Status:
UNKNOWN
Safety of Various Mode of Delivery of Iron Supplement on Iron Toxicity Markers in Preschool Children
Lead Sponsor:
Annamalai University
Conditions:
Iron Overload
Oxidative Stress
Eligibility:
All Genders
24-36 years
Phase:
PHASE3
Brief Summary
The purpose of study is to evaluate and compare the effect of iron supplementation when given as iron tablet or fortified biscuit or combined with zinc in the form of tablet on morbidity and iron toxi...
Detailed Description
The study will be carried out in two phases in Sangam Vihar, Delhi. The survey will be conducted to identify children in the age group of 24-36 months. After obtaining consent, an enrollment form with...
Eligibility Criteria
Inclusion
- between 24-36 months of age
- not severely malnourished or ill requiring hospitalization
- willing to stay in the study area for 6 months
- consent to participate
Exclusion
- not consented
- severely malnourished or ill requiring hospitalization
Key Trial Info
Start Date :
October 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
August 1 2010
Estimated Enrollment :
240 Patients enrolled
Trial Details
Trial ID
NCT00980421
Start Date
October 1 2009
End Date
August 1 2010
Last Update
September 21 2009
Active Locations (1)
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1
Center for Micronutrient Research
Delhi, National Capital Territory of Delhi, India, 110024