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Bioequivalence Study on Vitamin D in Healthy Adults

NCT03552653 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 31

Last updated 2018-06-12

No results posted yet for this study

Summary

The objective of this study is to evaluate and compare the bioequivalence between a single oral dose of vitamin D3 gummy vitamin versus vitamin D3 tablet in healthy adults.

Conditions

  • Measure Absorption of Vitamin D in Blood

Interventions

DIETARY_SUPPLEMENT

Vitafusion Extra Strength Vitamin D

Monitor Vitamin D blood levels

Sponsors & Collaborators

  • Medical University of South Carolina

    collaborator OTHER

  • Church & Dwight Company, Inc.

    lead INDUSTRY

Principal Investigators

  • Annahita Ghassemi · Church & Dwight Company, Inc.

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-08-26
Primary Completion
2017-12-22
Completion
2017-12-22

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03552653 on ClinicalTrials.gov