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Vitamin/Mineral Absorption From Two Different Supplements

Patterns of Plasma Vitamins and Minerals Following Intake of a Multivitamin/ Mineral Formula Produced by Two Different Manufacturing Processes

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05336994
Enrollment
17
Registered
2022-04-20
Start date
2022-04-29
Completion date
2022-07-30
Last updated
2022-09-02

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

Conditions

Healthy Nutrition

Keywords

Minerals, Vitamins, Absorption

Brief summary

The objective of this project is to evaluate the postprandial serum and plasma vitamin and mineral levels in healthy adult men and women between 18 and 32 years of age, following a single intake of a multivitamin and mineral supplement processed in two different ways.

Detailed description

Serum or plasma levels of five vitamins and four minerals will be measured at baseline, and 1, 2, 4, and 6 hours after the intake of a multivitamin/mineral supplement processed by two different methods. The two methods involve using either conventional isolated vitamins and minerals blended together to provide approximately 100% of the Daily Value, or using the same amount of vitamins and minerals that have first been processing into liposomal forms before blending. Participants are required to come for two study visits which are 5 to 7 days apart. Health screening will also be done at Study Visit 1. The order of supplement assignment will be randomized, performed in a double-blind manner.

Interventions

DIETARY_SUPPLEMENTMultivitamin/mineral supplement A

Oral administration of Supplement A

DIETARY_SUPPLEMENTMultivitamin/mineral supplement B

Oral administration of Supplement B

Sponsors

University of California, Davis
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Intervention model description

Participants will be randomly assigned to receive either supplement A or supplement B during the first visit. Five to seven days later, participants will receive the other supplement.

Eligibility

Sex/Gender
ALL
Age
18 Years to 32 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy males and females 18-32 years of age * BMI 18.5-32 kg/m2 * Free from disease * Normal blood levels in the comprehensive metabolic panel, or values slightly out of range as approved by the study physician * Normal blood pressure (individuals whose average blood pressure is greater than 140/90 will be excluded from the study) * Suitable vein structure and access for successful placement of an indwelling catheter, as determined by our nurse phlebotomist

Exclusion criteria

* Alcohol consumption \> 3 drinks/week (i.e., 1 bottle of beer, 1 glass of wine, and 1 shot of hard liquor) * Smoking * Vaping or using cannabis in any form * Using multivitamin/mineral supplements in the past two months * Currently taking supplements including botanical supplements, probiotics or fiber * Fruit consumption ≥ 2 cups/day * Vegetable consumption ≥ 3 cups/day * Coffee/tea ≥ 3 cups/day * Chronic/routine high-intensity exercise * Any chronic health conditions * Self-reported malabsorption * Currently taking prescription drugs * Indications of substance or alcohol abuse within the last 3 years * Unable to consent

Design outcomes

Primary

MeasureTime frameDescription
Assess the serum or plasma levels of five vitamins and four minerals6 hoursTotal area-under-the-curve of serum Vitamin A

Secondary

MeasureTime frameDescription
Assess the serum or plasma levels of five vitamins and four minerals6 hoursMaximum serum level of Vitamin A (mg/dL)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026