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NCT06010121

Comparison of Bioavailability of Liposomal and Traditional Formulation of Vitamin D3

Completed NA Last updated 25 August 2023
What this trial tests

NA trial testing Liposomal Vitamin D in Bioavailability of Vitamin D in 27 participants. Completed in 6 June 2023.

Timeline
17 February 2023
Primary endpoint
6 June 2023
6 June 2023

Quick facts

Lead sponsorAronPharma Sp. z o. o.
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingdouble
Primary purposeother
Enrollment27
Start date17 February 2023
Primary completion6 June 2023
Estimated completion6 June 2023
Sites1 location across Poland

Drugs / interventions tested

Conditions studied

Sponsor

AronPharma Sp. z o. o.

Who can join

Adults 18 to 60, any sex, with Bioavailability of Vitamin D. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other AronPharma Sp. z o. o. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06010121.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing