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Clinical Trial Summary

The recommended daily amounts of vitamins and minerals, referred to as micronutrients, are based on data from high income settings and for healthy populations do not fully correct nutritional deficiencies in undernourished settings. This study will determine the minimum acceptable doses across a range of nutrients at which sufficiency is achieved with supplementation using biochemical indicators of nutritional status in non-pregnant (non-lactating) women of reproductive age and pregnant women in Bangladesh. In this double-masked randomized controlled trial, a dose response study will be undertaken using increasing levels of doses provided as supplements to women (pregnant or non-pregnant) with nutritional indicators as outcomes.


Clinical Trial Description

The primary aims of the study are to: 1. To characterize the time-course of in vivo exposures (dose response) of several micronutrients in pregnant and non-pregnant and non-lactating women of reproductive age (WRA) in a real-life situation. 2. To characterize any clinically meaningful prognostic factors that can explain the between-subject variability. 3. To investigate whether the micronutrients follow dose-proportional pharmacokinetics. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06081114
Study type Interventional
Source Johns Hopkins Bloomberg School of Public Health
Contact Parul Christian, DrPH
Phone 4104194759
Email pchrist1@jhu.edu
Status Recruiting
Phase N/A
Start date October 22, 2023
Completion date September 30, 2025

See also
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