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Randomized Placebo-Controlled Trial (RPCT) of Maize/Zinc in Guatemala

Randomized Placebo-Controlled Trial (RPCT) of Maize/Zinc in Guatemala

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00098202
Enrollment
420
Registered
2004-12-06
Start date
2003-03-31
Completion date
2007-04-30
Last updated
2013-12-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nutrition, Pregnancy

Keywords

Global Network, Micronutrients, Zinc, Maternal and child health, Women's health, International, Guatemala, Nutrition, Corn, Maize

Brief summary

Malnutrition is a serious health problem in the developing world. This study looks at the effects of changing the type of basic food staple (corn) used in Guatemala and infant zinc supplementation on infants' growth, development, and illnesses from infectious diseases.

Detailed description

Poor mineral nutrition, especially deficiencies of iron and zinc, is a major cause of maternal and, especially, infant morbidity/mortality in developing world countries. The objectives of this study are to determine whether: a) linear growth velocity between 6 and 12 months in infants receiving a 5mg Zn supplement will be greater than that for infants receiving placebo; b) linear growth velocity will be greater for infants receiving complementary foods containing low phytate maize than for the infants fed wild-type control maize. In addition, Zn metabolic studies will be performed. The objective of the metabolic studies are to measure key variables of Zn homeostasis in maternal participants during changes in the reproductive cycle and in infants during a time when they are most vulnerable to Zn deficiency. The primary outcome measurement is linear growth velocity between 6 and 12 months. Secondary outcomes are weight gain, diarrheal incidence/prevalence and infant neurodevelopmental measures. Optional maternal and infant biochemical data will be collected from a convenience sample comprised of willing participants. One additional component to this study is to collect information on the nutritional status of the women receiving low-phytate vs. control maize and the infants enrolled in this study. The current protocol for infants in this study specifies measurements of exchangeable zinc pool (EZP) at 6 and 12 months of age; in order to lessen the burden of study participation we plan to conduct the metabolic studies in infants at only nine months of age. In addition to decreasing the number of infant studies, this change will enable families who are only participating in the metabolic studies (not simultaneously enrolled in the sibling cohort) to cease all study demands at the end of the nine month measurement (an overall decrease of three months in study participation). The primary outcome measure for this study is the quantity of zinc absorbed (mg/day)from complementary foods and a Zn supplement at age 9 months. The rationale for measures of zinc absorption in infants is that the low phytate complementary feeding is expected to have a beneficial public health effect only if it results in enhanced mineral, especially zinc, absorption. Therefore, confirmation of increased zinc absorption can be regarded as the first logical stage of any efficacy study. The sample size of 420 is required in order to observe a 6% increase in growth rates for Zn supplemented infants compared to placebo treated infants within each maize group with 80% power.

Interventions

DRUGLow phytic acid maize
DRUGZinc

Sponsors

Global Network for Women's and Children's Health Research
CollaboratorOTHER
Bill and Melinda Gates Foundation
CollaboratorOTHER
Fogarty International Center of the National Institute of Health
CollaboratorNIH
National Center for Complementary and Integrative Health (NCCIH)
CollaboratorNIH
National Institute of Dental and Craniofacial Research (NIDCR)
CollaboratorNIH
National Cancer Institute (NCI)
CollaboratorNIH
RTI International
CollaboratorOTHER
University of Colorado, Denver
CollaboratorOTHER
Center for Studies of Sensory Impairment, Aging and Metabolism
CollaboratorOTHER
Foundation for Alimentation and Nutrition, Central America and Panama
CollaboratorOTHER
USDA Beltsville Human Nutrition Research Center
CollaboratorFED
NICHD Global Network for Women's and Children's Health
Lead SponsorNETWORK

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
DOUBLE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Informed consent of mother * Mother between the ages of 18 and 40 years * Mother typically eats homemade tortillas * Mother typically eats a minimum of 15 homemade tortillas per day. * Mother resides in a community served by the Comalapa, Chimaltenango, Community Health Center in the Western Highlands of Guatemala

Exclusion criteria

* Other member of the dwelling unti already enrolled in the study. * Mother has more than eight living children.

Design outcomes

Primary

MeasureTime frame
Infant Maize/Zn Supplementation Trial:
Linear growth velocity
Zn Homeostasis Studies:
Measures of zinc homeostasis

Secondary

MeasureTime frame
Infant Maize/Zn Supplementation Trial:
Maternal and infant biomarkers
Weight gain
Morbidity
Infant neurodevelopment

Countries

Guatemala

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026