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Evaluation of a Transdermal Vitamin D3 Delivery System, D3forME

NCT02174718 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2018-11-02

No results posted yet for this study

Summary

A clinical need exists for non-oral vitamin D administration. This study is designed to test a new proprietary transdermal system. It is looking to see if this new system will safely and successfully deliver vitamin D3 to humans.

Conditions

  • Vitamin D Deficiency

Interventions

DIETARY_SUPPLEMENT

Transdermal D Patch

DIETARY_SUPPLEMENT

Oral vitamin D3

DIETARY_SUPPLEMENT

Placebo patch

DIETARY_SUPPLEMENT

Oral placebo

Sponsors & Collaborators

  • University of Wisconsin, Madison

    lead OTHER

Principal Investigators

  • Neil Binkley, M.D. · University of Wisconsin, Madison

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2015-11-30
Primary Completion
2017-11-30
Completion
2017-11-30

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 NCT02174718 on ClinicalTrials.gov