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Examination of the relevance of plant products on vitamin B12-supply of vegetarians and vegans

Examination of the relevance of plant products on vitamin B12-supply of vegetarians and vegans - PflB12-Veg

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00009974
Enrollment
90
Registered
2016-02-11
Start date
2015-12-01
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

VITAMIN B12 MALNUTRITION

Interventions

Group 1: Vegan dietary supplement containing synthetic vitamin B12
Dosage: 1 pill daily = 2,5 µg vitamin B12/day
intake over a period of eight weeks Group 2: Vegan dietary supplement containing pure Chlorella vulgaris
Dosage: 8 pills daily = 2,5 µg vitamin B12/day
intake over a period of eight weeks Group 3: Vegan dietary supplement containing primarily sea buckthorn, quinoa, quitch
Dosage: 9g/day = 2,5 µg vitamin B12/day)
intake over a period of eight weeks

Sponsors

Institut für Lebensmittelwissenschaft und Humanernährung
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Non-smokers; vegetarian and / or vegan diet for at least 1 years; serum cobalamin range between 110-310 pmol/l; written consent after information about study contents and study procedure; Ability and willingness of study participants to follow study leaders instructions

Exclusion criteria

Exclusion criteria: Intake of vitamin B12-containing dietary supplements 3 month before study begin; severe chronic illness (Cancer, diabetes mellitus Typ I, manifest coronary heart disease), severe kidney or liver diseases; Allergies or intolerances regarding study product contents; chronic gastroinestinal diseases (especially small intestine e.g. duodenal ulcer, liver, pancreas) and state after gastrointestinal surgical procedure e.g. nontropical sprue, short bowel syndrome); Heart or gastrointestinal surgery; immediate planned surgery; BMI >30 kg/m²; addiction to alcohol and/or drugs; smoking; Pregnancy and lactation; missing consent or refusing / reset of the consent

Design outcomes

Primary

MeasureTime frame
Changes in holotranscobalamin (week 8 (t8) in comparison to week 4 (t4); week 8 (t8) in comparison to baseline (t0); week 4 (t4) in comparison to baseline (t0)) (blood parameter)

Secondary

MeasureTime frame
Changes in serum cobalamin (week 8 (t8) in comparison to week 4 (t4); week 8 (t8) in comparison to baseline (t0); week 4 (t4) in comparison to baseline (t0)) (blood parameter); Changes in methylmalonic acid (week 8 (t8) in comparison to week 4 (t4); week 8 (t8) in comparison to baseline (t0); week 4 (t4) in comparison to baseline (t0)) (blood parameter); Changes in folic acid (week 8 (t8) in comparison to week 4 (t4); week 8 (t8) in comparison to baseline (t0); week 4 (t4) in comparison to baseline (t0)) (blood parameter)

Countries

Germany

Contacts

Public ContactIsabel Behrendt

Institut für Lebensmittelwissenschaft und Humanernährung

behrendt@nutrition.uni-hannover.de0511 762 3317

Outcome results

None listed

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