Clinical Trials Directory

Trials / Completed

CompletedNCT02158598

Comparison of Changes in Serum 25(OH)D Concentrations Following Vitamin D Supplementation With Chewable Tablets Versus Pills

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
38 (actual)
Sponsor
CHU de Quebec-Universite Laval · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

This is a 6-month cross-over trial of vitamin D supplementation in 38 healthy men and women aged 18 years and older. The primary aim is to compare the change in serum 25(OH)D concentration following vitamin D supplementation with chewable tablets versus pills. Secondary aims are to evaluate satisfaction and adherence to the vitamin D chewable tablet supplement. Questionnaires on physical activity, sunlight exposure and dairy product consumption will be administered to adjust for confounding factors. A questionnaire will be administered to assess satisfaction and pill count to evaluate adherence to treatment. This research intends to test the hypothesis that the vitamin D chewable tablet supplement is as effective as a traditional vitamin D pill supplement to increase serum 25(OH)D concentrations.

Conditions

Interventions

TypeNameDescription
DRUGVitamin D chewable tablet supplementation
DRUGVitamin D pill supplementation

Timeline

Start date
2014-06-01
Primary completion
2017-12-01
Completion
2018-05-09
First posted
2014-06-09
Last updated
2018-07-30

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT02158598. Inclusion in this directory is not an endorsement.