NCT05898217

Vitamin and Mineral Absorption From Milk and PBMAs

Relative Absorption of Fat-soluble Vitamin D and Minerals From Select Plant-based Milks in Human Subjects
Clinical Nutrition Research Center, Illinois Institute of Technology·ClinicalTrials.gov·otherNot yet recruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Nutrition, Healthy
Drug/Device/Intervention
Dairy Milk
Study type
Interventional
Intervention type
other
Sponsor & location
Primary sponsor
Clinical Nutrition Research Center, Illinois Institute of Technology
Location
Chicago, United States of America
Timeline & enrollment
Phase
N/A
Start date
Jun 01, 2023
End date
May 30, 2025
Enrollment
60 participants
Primary outcome

Concentration of vitamin D in plasma/serum,Concentration of calcium, potassium, and magnesium in human serum and urine

Summary

Plant-based milk alternatives (PBMAs) are a popular alternative to cow's milk. The different
 types of PBMAs on the market shelf include almond, oat, soy, coconut, cashew, pea, hemp, and
 rice. Among these, PBMA made from almonds, oats and soy are the most popular in North
 America. Though PBMAs are designed to mimic cow's milk in terms of color, they often have a
 very different nutrition profile. In order to better substitute for cow's milk, PBMAs often
 have added vitamins and minerals, as well as added sugars and flavorings to improve flavor.
 
 This study will test how well certain nutrients (vitamin D, calcium, potassium, and
 magnesium) are absorbed by the body after intake of milk and PBMAs. Nutrient absorption will
 be measured using blood samples after short term intake (from 1 hours to 1 week) of almond,
 soy, and oat milk, and compare it to cow's milk. Participants in the study will avoid all
 fluid dairy products and vitamin-D supplemented foods for three weeks and then be asked to
 consume either almond, soy, oat, or cow's milk for one week.
 
 All participants will visit the Clinical Nutrition Research Center (CNRC) four times over the
 course of about one month. These visits include a screening and pre-study visit (1.5 hrs), a
 pick-up visit (30 min), one long study day visit (~11 hours), and two shorter follow up study
 day visits (1 hr).

ICD-10 classifications
Seeking and accepting physical, nutritional and chemical interventions known to be hazardous and harmfulMalnutritionObesitySequelae of malnutrition and other nutritional deficienciesNutritional deficiency, unspecified
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT05898217
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT05898217 through Pure Global AI's free database. This phase not specified trial is sponsored by Clinical Nutrition Research Center, Illinois Institute of Technology and is currently Not yet recruiting. The study focuses on Nutrition, Healthy. Target enrollment is 60 participants.

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