NCT06372158

Effects of Liposomal Encapsulation on Calcium Powder Absorption and Metabolism

National Yang Ming University·ClinicalTrials.gov·dietary supplementRecruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Osteoporosis
Drug/Device/Intervention
Stage 1
Study type
Interventional
Intervention type
dietary supplement
Sponsor & location
Primary sponsor
National Yang Ming University
Location
Taipei,Taipei, Taiwan
Timeline & enrollment
Phase
N/A
Start date
Apr 08, 2024
End date
Dec 01, 2024
Enrollment
20 participants
Primary outcome

General examination,Hematology Test

Summary

Compared with traditional calcium supplements, liposome calcium can increase the
 bioavailability of calcium and reduce the waste caused by gastric acid destruction of
 calcium. This allows calcium to be released slowly in the intestines, reducing the risk of
 indigestion or other side effects caused by excessive intake at one time. Liposomal calcium
 can be taken orally directly. It does not need to be dissolved in water before taking like
 other calcium supplements, making it more convenient to use. Based on the above advantages,
 liposomal calcium is a relatively safe and easy-to-absorb calcium supplement, suitable for
 long-term use, and can meet the body's demand for calcium. According to the recommendations
 of the World Health Organization, the daily calcium intake for adults should be 1000-1300 mg.
 In Taiwan, the seventh edition of the revised reference intake of dietary nutrients for
 Chinese people recommends that the daily intake for adults should be 1,000 mg. The calcium
 dose used in this study was 500 mg. The purpose was to explore whether the sustained-release
 characteristics of liposome coating technology can improve the absorption rate after
 consuming calcium powder and achieve better bioavailability. It is expected that microlipids
 made by lecithin can Lipid calcium powder increases its maintenance time in the blood,
 thereby increasing the supplementary effect of calcium, and is an alternative to calcium
 supplements.

ICD-10 classifications
Osteoporosis, unspecifiedOther osteoporosisIdiopathic osteoporosisOsteoporosis in diseases classified elsewherePostmenopausal osteoporosis
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06372158
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06372158 through Pure Global AI's free database. This phase not specified trial is sponsored by National Yang Ming University and is currently Recruiting. The study focuses on Osteoporosis. Target enrollment is 20 participants.

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