ClinicalTrials.Veeva

Menu

Effect of Iron/Zinc-Biofortified Pearl Millet on Growth and Immunity in Children Aged 12-18 Months in India

C

Cornell University

Status

Completed

Conditions

Iron Deficiency
Zinc Deficiency

Treatments

Other: FeZnPM
Other: CtrlPM

Study type

Interventional

Funder types

Other

Identifiers

NCT02233764
IRB #: 1403004556

Details and patient eligibility

About

In this study, iron- and zinc-biofortified pearl millet will be fed to young children in Mumbai, Maharashtra, India over a period of nine months to measure growth and immune function in comparison to children receiving non-biofortified pearl millet.

Full description

Iron and zinc deficiency remain a major worldwide public health problem, especially in developing countries such as India. In this randomized study, 700 children aged 12-18 months from Mumbai, Maharashtra, India will be fed either iron and zinc biofortified pearl millet or control pearl millet three times per day, six days per week, for nine months. The goal of this study is to examine the effects of iron and zinc biofortified millet on immune function, growth, and cognitive function in this age group. The key outcome measures are biomarkers of iron and zinc status, growth, and immune function. Serum concentrations of hemoglobin, ferritin, serum transferrin receptor, and zinc will be assessed at enrollment (baseline), at an intermediate time point (midline; random serial sampling) and after 9 months of follow-up (endline). Additionally, we will measure concentrations of C-reactive protein (CRP) and alpha 1-acid glycoprotein (AGP), as iron and zinc biomarkers can be influenced by inflammation. To assess cognitive function in a subset, multiple specific aspects of memory, attention, and processing speed will be assessed. Higher-level, integrative cognitive abilities that require the coordination of multiple specific functions, such as problem-solving and exploratory behavior and global aspects of attention during free play with toys, will also be assessed.

Enrollment

223 patients

Sex

All

Ages

12 to 18 months old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 12 months, 0 days to 18 months, 30 days (at time of screening/baseline visit)
  • Hemoglobin ≥9 g/dL

Exclusion criteria

  • Age less than 12 months, 0 days or older than 18 months, 30 days (at time of screening/baseline visit)
  • Hemoglobin < 9 g/dL and/or hemoglobinopathy
  • Presence of severe malnutrition according to Wellcome Classification (marasmus, marasmic kwashiorkor, kwashiorkor, weight-for-height z-score < -3)
  • Prior diagnoses of HIV/AIDS or Tuberculosis, or Current diagnosis of HIV/AIDS, malaria, Dengue fever, Tuberculosis requiring >1 day hospitalization
  • Children who do not have a caretaker to bring him/her to feeding center
  • Possibility of migrating out of the slum dwelling for longer than 4 weeks
  • Prior or current consumption of iron or zinc supplements in the past 1 year
  • Any known dietary allergies

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

223 participants in 2 patient groups

FeZnPM
Experimental group
Description:
The FeZnPM arm will consume iron- and zinc-biofortified pearl millet (ICTP8203-Fe).
Treatment:
Other: FeZnPM
CtrlPM
Active Comparator group
Description:
The CtrlPM arm will consume conventional pearl millet three times per day, six days per week, for 9 months. Children are anticipated to consume 25-30 grams of the pearl millet at each feeding. The pearl millet will be prepared using a variety of recipes such as porridges, breads, and biscuits.
Treatment:
Other: CtrlPM

Trial contacts and locations

3

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems