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Bioavailability of zinc from milk and rice using a stable isotope method

Bioavailability of zinc from milk and rice using a stable isotope method

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON21804
Enrollment
38
Registered
2013-11-18
Start date
2014-01-06
Completion date
Unknown
Last updated
2024-06-11

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

Conditions

bioavailability, biobeschikbaarheid absorption, absorptie

Interventions

Study I: Intake of 1. milk 2. Zn-fortified milk 3. water + Zn supplement 4. raw milk All test meals are extrinsically labelled with 67Zn. Study II: Intake of 1. intrinsically 67Zn label

Sponsors

Wageningen University Division of Human Nutrition
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Female • Age between 18-30 years of age (boundaries included) • Body Mass Index (BMI) between 19-25 kg/m2 (boundaries included) • Body weight between 60-70 kg (boundaries included) • No mineral and vitamin supplements two weeks prior to the 1st test meal and during the whole duration of the study • Willing to abstain from blood donation during the study • Voluntary participation • Signed informed consent • Willing to comply with the study procedures

Exclusion criteria

Exclusion criteria: • Any metabolic, gastrointestinal, inflammatory or chronic disease or disorder (such as diabetes, anaemia, hepatitis, hypertension, cancer or cardiovascular diseases; according to the subjects own statement) • Continuous/long-term medication during the whole study (except for contraceptives) • Mineral or vitamin supplements during the 2 weeks prior to 1st test meal • Lactose intolerance • Alcohol consumption > 21 glasses per week • Bad venous access • Reported weight loss or gain of > 2 kg in the last month before screening • Reported strictly prescribed diet, vegetarian, vegan or macrobiotic • Smoking • Pregnant or lactating or the wish to become pregnant in the study period (a pregnancy test will be done at screening) • Lack of safe contraception • Earlier participation in any nutrition study using Zn stable isotopes as well as participation in any other clinical study within the last 30 days and during this study

Design outcomes

Primary

MeasureTime frame
Fractional absorption of Zn, as measured from isotope ratios in urine samples.

Secondary

MeasureTime frame
• Zn status in blood • Inflammation markers(C-reactive protein (CRP) and á-glycoprotein (AGP)) in blood.

Contacts

Public ContactEsther Boelsma

Wageningen UR Food & Biobased Research Bornse Weilanden 9

esther.boelsma@wur.nl+31 317 480309

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)