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Comparison of Bioavailability of Liposomal and Traditional Formulation of Vitamin D3

NCT06010121 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 27

Last updated 2023-08-25

No results posted yet for this study

Summary

The aim of the study was to compare the profiles of 25-hydroxyvitamin D serum concentration in healthy adults after 4 weeks of using vitamin D supplementation either in a liposomal or a traditional formulation.

Conditions

  • Bioavailability of Vitamin D

Interventions

DIETARY_SUPPLEMENT

Liposomal Vitamin D

2000 IU of cholecalciferol in liposomal formulation

DIETARY_SUPPLEMENT

Traditional Vitamin D

2000 IU of cholecalciferol in traditional formulation

Sponsors & Collaborators

  • AronPharma Sp. z o. o.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-02-17
Primary Completion
2023-06-06
Completion
2023-06-06

Countries

  • Poland

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 NCT06010121 on ClinicalTrials.gov