ClinicalTrials.Veeva

Menu

Vitamin/Mineral Absorption From Two Different Supplements

University of California (UC) Davis logo

University of California (UC) Davis

Status

Completed

Conditions

Healthy Nutrition

Treatments

Dietary Supplement: Multivitamin/mineral supplement B
Dietary Supplement: Multivitamin/mineral supplement A

Study type

Interventional

Funder types

Other

Identifiers

NCT05336994
1692409

Details and patient eligibility

About

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.

Full 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.

Enrollment

17 patients

Sex

All

Ages

18 to 32 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Quadruple Blind

17 participants in 2 patient groups

Multivitamin/mineral supplement A to B
Experimental group
Description:
Participants will be randomly assigned to receive Supplement A and after 5-7 days of follow-up, they will receive Supplement B.
Treatment:
Dietary Supplement: Multivitamin/mineral supplement A
Dietary Supplement: Multivitamin/mineral supplement B
Multivitamin/mineral supplement B to A
Experimental group
Description:
Participants will be randomly assigned to receive Supplement B and after 5-7 days of follow-up, they will receive Supplement A.
Treatment:
Dietary Supplement: Multivitamin/mineral supplement A
Dietary Supplement: Multivitamin/mineral supplement B

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems