- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05061290
Iron Bioavailability From Cereal-based Foods
The Potential of Food to Food Fortification to Improve Iron Bioavailability From Cereal-based Foods
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
To better understand the potential for leveraging traditional plant-based ingredients in local fortification efforts in Africa, the proposed study will focus on assessment of acute iron bioavailability in participants consuming instant blended cereal porridges produced using whole grain white maize, with provitamin A (e.g. carrots/mango), moringa leaf powder and baobab fruit powder in specific combinations. The investigators hypothesize that: food-to-food fortified cereal-based porridge with with African baobab fruit and moringa leaf powder will effectively improve iron density and bioavailability in human participants as compared to a "gold standard" fortification (iron sulphate and ascorbic acid).
A randomized crossover design with 4 different white maize cereal-based porridges and a reference control porridge (with matching macronutrient contents) will be used, allowing each participant to serve as their own control. Porridges are designed to specifically compare: (1) Food to food fortification versus standard fortifications and (2) the ability of baobab fruit pulp to enhance iron absorption from both natural and standard sources. The porridges will be composed of locally sourced ingredients including: whole grain white maize, a pro-vitamin A source (oil and available vegetables e.g. carrot and mango) baobab fruit powder and moringa leaf powder.
The enrolled participants will come into the clinic 6 times to consume porridges or have blood drawn. Four times blood (1 for screening, 3 for study) will be drawn to determine the amount of the different forms of iron in participant's blood. On each day of porridge consumption (each visit except the final visit on Day 33), they will consume 2 x 350 g porridge meals and stay 90 mins after the participant has finished each of the meals, and then leave and come back to repeat for a total of 4 hours. After two weeks they will return to the clinic and the investigators will ask to draw some more blood to see if they have absorbed any of the different forms of iron. They will then have the next porridge. Importantly for each visit for both blood draws and the porridge consumption the participants will have to fast the previous night, so no food or beverages like tea or coffee can be consumed (only water allowed). During 5 visits when they will eat two portions of porridge during the day and will have to stay at the facility for 90 mins after each porridge consumption. During the last visit (Day 33), participants will need to give a blood sample, which will take about half an hour. Blood collected during these visits will be used to measure isotopic iron absorbed from the porridges.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Bruce Hamaker
- Phone Number: 7654945668
- Email: hamakerb@purdue.edu
Study Locations
-
-
Indiana
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West Lafayette, Indiana, United States, 47907
- Purdue University
-
Contact:
- Bruce R Hamaker, PhD
- Phone Number: 765-494-5668
- Email: hamakerb@purdue.edu
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion:
- Female 18-65 Y
- BMI 18.5-25 kg/m2
- Stable weight past 3 month (+/- 2.5kg)
- Clinically normal blood profiles
- Fasting blood glucose < 110 and CRP below 3 mg/L
Exclusion:
- Smokers and vapers
- No heavy alcohol consumption (>2 drinks per day)
- Diabetic
- Presence of metabolic of intestinal disorder including lipid malabsorption or lactose intolerance
- Male sex
- Pregnant
- Lactating
- Long term use of medications
- Blood donation in past 4 months
- Previous participation in iron stable isotope bioavailability study
- Following a weight reduction program or having one in past 3 months
- Peri- or post-menopausal
- Acute or chronic disease
- Hypertension
Study Plan
How is the study designed?
Design Details
- Primary Purpose: BASIC_SCIENCE
- Allocation: RANDOMIZED
- Interventional Model: CROSSOVER
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Control Porridge
Wholegrain maize flour, Mango powder, Carrot powder, Ferrous sulfate, Corn starch
|
Maize porridge containing 54Fe as iron sulfate
|
|
EXPERIMENTAL: Reference Porride A
Wholegrain maize flour, Mango powder, Carrot powder, Ferrous sulfate, Ascorbic acid, Corn starch
|
Maize porridge counting 58Fe as iron sulfate with ascorbic acid
|
|
EXPERIMENTAL: Test Porridge B
Wholegrain maize flour, Moringa leaf powder, Mango powder, Carrot powder, Corn starch
|
Maize porridge containing 57Fe and fortified with Moringa leaf powder as iron source
|
|
EXPERIMENTAL: Test Porridge C
Wholegrain maize flour, Baobab fruit powder, Mango powder, Carrot powder, Ferrous sulfate, Corn starch
|
Maize porridge containing 57Fe and fortified with Boabab fruit powder as iron source
|
|
EXPERIMENTAL: Test Porridge D
Wholegrain maize flour, Baobab fruit powder, Moringa leaf powder, Mango powder, Carrot powder
|
Maize porridge containing 54Fe and fortified with Moringa leaf and Baobab fruit powder as iron source
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Iron absorption
Time Frame: Acute study but blood measurement to occur following 14 daysof acute consumption
|
Assessment whole blood for isotopic iron absorption from individual meals
|
Acute study but blood measurement to occur following 14 daysof acute consumption
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ANTICIPATED)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- IRB-2019-764
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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