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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01990872
Other study ID # PR-IC-1111-10005
Secondary ID
Status Completed
Phase N/A
First received November 8, 2013
Last updated November 21, 2013
Start date October 2012
Est. completion date November 2013

Study information

Verified date November 2013
Source University College Cork
Contact n/a
Is FDA regulated No
Health authority Ireland: Irish Medicines Board
Study type Interventional

Clinical Trial Summary

This winter-based placebo-controlled, single-dose vitamin D randomized controlled trial (RCT) aims to examine the impact of various levels of habitual calcium intake on dietary vitamin D requirements in older adults stratified by calcium intake. This will provide new data on the impact of different levels of calcium intake, ranging from low/moderate to high, on winter serum 25(OH)D levels, and their utilization and catabolism in adults.


Description:

The aim of this study is to perform a randomised controlled vitamin D3 intervention study in apparently healthy, free-living adults (aged 50+ y) to investigate whether different levels of habitual calcium intake, ranging from low-moderate to high, influence serum 25(OH)D concentrations and indices of vitamin D activation and catabolism during winter, when vitamin D intake is adequate versus inadequate.

This research will provide new data and scientific understanding in relation to the impact of different levels of dietary calcium intake on vitamin D requirements in the older adult population. As such, this new data will inform dietary reference values for vitamin D.


Recruitment information / eligibility

Status Completed
Enrollment 125
Est. completion date November 2013
Est. primary completion date November 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 50 Years to 80 Years
Eligibility Inclusion Criteria:

Consenting white men and women aged = 50 y

Exclusion Criteria:

- Unwilling to discontinue consumption of vitamin D-containing supplements 4 wks before the initiation of the study and throughout the study.

- Planning to take a winter vacation (during the course of the 15-wk intervention) to a location at which either the altitude or the latitude was predicted to result in significant cutaneous vitamin D synthesis from solar radiation (e.g., a winter sun coastal resort or a mountain ski resort)

- Use of tanning facilities of any type.

- Pregnancy or planning to become pregnant during the study

- A severe medical illness,

- hypercalcaemia,

- Known intestinal malabsorption syndrome,

- Excessive alcohol use,

- Taking medications known to interfere with vitamin D metabolism

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Vitamin D3 (20 micrograms/day)
Vitamin D3 (20 micrograms/day)
Placebo
Placebo (0 micrograms vitamin D3/day)

Locations

Country Name City State
Ireland Human Dietary Studies Facility, School of Food and Nutritional Sciences, University College Cork, Cork, Ireland Cork

Sponsors (1)

Lead Sponsor Collaborator
University College Cork

Country where clinical trial is conducted

Ireland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Response of serum 25(OH)D concentration over winter in subjects stratified by calcium intake 0, 8, 15 weeks No
Secondary Serum albumin-adjusted calcium 0, 8, 15 weeks Yes
Secondary serum parathyroid hormone 0, 8, 15 weeks No
Secondary Serum 24,25(OH)2D 0 and 15 weeks No
Secondary Serum 1,25(OH)2D 0 and 15 weeks No
Secondary Serum free 25(OH)D 0 and 15 weeks No
Secondary Serum vitamin D binding protein 0 and 15 weeks No
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