Evaluation of the Effect of Body Weight and Composition on Iron Absorption and Blood Volume
NCT ID: NCT01884506
Last Updated: 2013-10-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
64 participants
INTERVENTIONAL
2013-06-30
2013-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
BASIC_SCIENCE
DOUBLE
Study Groups
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labeled iron meal
Test meal (bread with honey) with a labeled iron solution
labeled iron solution
labeled iron as ferrous sulfate (6mg/test meal)
labeled iron solution and ascorbic acid
labeled iron as ferrous sulfate plus ascorbic acid (6mg:30mg /test meal)
labeled iron and ascorbic acid meal
Test meal (bread with honey) with a labeled iron solution and ascorbic acid
labeled iron solution
labeled iron as ferrous sulfate (6mg/test meal)
labeled iron solution and ascorbic acid
labeled iron as ferrous sulfate plus ascorbic acid (6mg:30mg /test meal)
Interventions
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labeled iron solution
labeled iron as ferrous sulfate (6mg/test meal)
labeled iron solution and ascorbic acid
labeled iron as ferrous sulfate plus ascorbic acid (6mg:30mg /test meal)
Eligibility Criteria
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Inclusion Criteria
* Age 18-45 years
* Pre-menopausal (no absence of a menstrual cycle in the past 12 months)
* BMI 18.5-39.9 kg/m2 (n=25 18.5-24.9, n=25 25-29.9, n=25 30-39.9)
* Apparently healthy (no significant medical conditions that could influence iron or inflammatory status other than obesity (i.e., cancer, HIV/AIDS, inflammatory bowel disease, gastrointestinal bleeding, and rheumatoid arthritis, renal disease or hemochromatosis) (judged by study physician)
Exclusion Criteria
* Use of medication which interferes with study measurements (judged by the study physician)
* Smoking
* Pregnancy and lactation; planning to become pregnant during the course of the study (pregnancy test will be conducted at visit 2 and subjects will be asked about contraception\*)
* Consumption of vitamin- or mineral supplements unless they consent to discontinue intake two weeks before the start of the study until the final blood sampling
* Prior participation in studies using stable iron isotopes
* Food allergies/intolerances (gluten, lactose, milk protein)
* Blood donation during the two months prior to the study
* Major injuries during the 6 months prior to the study
* Illness during the 4 weeks prior to the study (judged by study physician)
* Administration of recombinant erythropoietin (rhEPO)
* More than 5 days at altitudes above 1600 m above sea level during the 3 weeks prior to the study
* Long distance flight (\>8 h) during the 3 weeks prior to the study
* Chronic alcohol abuse
18 Years
45 Years
FEMALE
Yes
Sponsors
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Wageningen University
OTHER
Universidad de Monterrey
OTHER
Swiss Federal Institute of Technology
OTHER
Responsible Party
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Prof. Michael B. Zimmermann
Prof. Dr.
Principal Investigators
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Isabelle Aeberli, PhD
Role: PRINCIPAL_INVESTIGATOR
ETH Zurich
Locations
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Human Nutrition Laboratory, ETH Zurich
Zurich, , Switzerland
Countries
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References
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Cepeda-Lopez AC, Melse-Boonstra A, Zimmermann MB, Herter-Aeberli I. In overweight and obese women, dietary iron absorption is reduced and the enhancement of iron absorption by ascorbic acid is one-half that in normal-weight women. Am J Clin Nutr. 2015 Dec;102(6):1389-97. doi: 10.3945/ajcn.114.099218. Epub 2015 Nov 11.
Other Identifiers
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KEKZH-2013-0110
Identifier Type: -
Identifier Source: org_study_id