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Method development - markers for the intake of selected plant foods

Method development - markers for the intake of selected plant foods - FoodPhyt-MarVeL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00029266
Enrollment
15
Registered
2022-08-03
Start date
2022-06-29
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Healthy participants

Interventions

Group 1: foods visit 1
volunteer01 combination 1
volunteer02 zuccini
volunteer03 carrot
volunteer04 combination 3
volunteer05 spinach
volunteer06 zuccini
volunteer07 kiwi
volunteer08 peas
volunteer09 spinach
volunteer10 peas
volunteer11 cucumber
volunteer12 kiwi
volunteer13 combination 1
volunteer14 combination 2
volunteer15 green beans
combination 1 = salat of fruits (blueberries, strawberries, orange, banana, grape, pear, apple) and coffee
combination 2 = salat white cabbage, red cabbage, broccoli, cauliflower, kohlrabi, onion, olive oil, tomato, mushrooms, potato, walnuts and red wine
combination 3 = wholegrain crispbreads, dark chocolate and black tea Group 2: foods visit 2
volunteer01 cucumber

Sponsors

Max Rubner-Institut; Bundesforschungsinstitut für Ernährung und Lebensmittel
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: - Healthy women and men (18-40 years) - BMI 18.5 - 30 kg/m2 - Good health status - Written informed consent to participate in the study - No medical conditions affecting nutrient absorption, digestive function, metabolism or excretion - Non-smoker - No regular use of medication (except hormonal contraceptives) - No intake of antibiotics in the previous 6 months - No intake of nutritional supplements in the preceding 4 weeks - No pregnancy or lactation period - No allergy/ intolerance to food or ingredients of the test meals

Exclusion criteria

Exclusion criteria: - Need to take certain medications during the trial period; the assessment is made by the study physician - Occurrence of unacceptable adverse events - Withdrawal of consent to participate in the study - Non-compliance with the instructions in the study protocol (including hygiene measures) the hygiene measures)

Design outcomes

Primary

MeasureTime frame
Analysis of the specific increase or specific occurrence of metabolites/marker candidates in urine derived from the tested plant food after a single consumption of the test food compared to the fasting urine sample using untargeted LC-MS-based metabolomics methods.

Secondary

MeasureTime frame
Determination of the expected concentration range for the selected marker candidates in the urine of participants, and, if possible, identification of new marker candidates in the urine for the consumed foods using LC-MS based methods.

Countries

Germany

Contacts

Public ContactMaria Herrmann

Max-Rubner-Institut Bundesforschungsinstitut für Ernährung und Lebensmittel

studienzentrum@mri.bund.de0721/6625-400

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026