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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02008201
Other study ID # D-status
Secondary ID
Status Completed
Phase Phase 3
First received September 10, 2013
Last updated December 12, 2014
Start date May 2012
Est. completion date April 2014

Study information

Verified date December 2013
Source Wageningen University
Contact n/a
Is FDA regulated No
Health authority Netherlands: Medical Ethics Review Committee (METC)
Study type Interventional

Clinical Trial Summary

The objectives of this study are 1) to assess the prevalence of vitamin D deficiency in a group of sub elite athletes and 2) to identify seasonal changes in vitamin D status and the effect that supplementation may have during the course of a year.

The study is a double blinded parallel study design.


Description:

Study population: 175 elite/ sub elite athletes, male and female, aged 18-60y, from a variety of sport disciplines


Recruitment information / eligibility

Status Completed
Enrollment 153
Est. completion date April 2014
Est. primary completion date April 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- athletes

- 19-60y

Exclusion Criteria:

- subjects who take vitamin D supplements

Study Design

Allocation: Randomized, Endpoint Classification: Bio-availability Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
vitamin D


Locations

Country Name City State
Netherlands Wageningen University Wageningen

Sponsors (1)

Lead Sponsor Collaborator
Wageningen University

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in serum 25(OH)D Every 3 months during one year No
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