Absorption Kinetics and Efficacy of Vitamin D Enriched Supplements in Older Adults.

Vitamin D Deficiency Clinical Trial

Official title: Absorption Kinetics and Efficacy of Vitamin D Enriched Supplements in Older Adults.

Status Completed

Clinical Trial Summary

The proposed study will examine vitamin D bioavailability when 20µg of vitamin D is consumed in 5 different forms:

i) a vitamin D enriched pre-formed mixed micelle dairy drink ii) a vitamin D enriched olive oil dairy drink iii) a vitamin D enriched fish oil dairy drink iv) a vitamin D enriched fat-free dairy drink

Clinical Trial Description

This postprandial study will recruit healthy males and females aged 18 and over. Upon completion of informed consent procedures and successful screening, the volunteers will complete 4 study visits. Participants will consume a standardised meal the evening before each test day, and will arrive in the morning to the research facility in UCD after an overnight fast of 12 hours.

On the study test days, volunteers will be given one of the following vitamin D treatments in a dairy drink, followed by a low-fat breakfast.

1. mixed micelles

2. olive oil

3. fish oil

4. fat-free

Participants will also be given a low-fat lunch 5 hours after the supplement is consumed. Volunteers will be cannulated by a trained phlebotomist on arrival, and a fasting blood sample will be taken. Following ingestion of the vitamin D supplements blood samples will be taken at 0,2,4,6, and 8 hours post ingestion. A 10mL sample will be collected at each time point. In total, 60mL of blood will be collected over 24 hours. The participant's food intake will be recorded during the visit. ;

Related Conditions & MeSH terms

• Vitamin D Deficiency

• NCT number: NCT04935034
• Study type: Interventional
• Source: University College Dublin
• Status: Completed
• Phase: N/A
• Start date: July 1, 2018
• Completion date: May 31, 2021