Clinical Trials Directory

Trials / Completed

CompletedNCT05843617

Comparison of Bioavailability of Liposomal and Traditional Formulation of Vitamin C

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
10 (actual)
Sponsor
AronPharma Sp. z o. o. · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

The aim of the study was to compare the profiles of vitamin C serum concentration in healthy volunteers after the single oral administration either in a liposomal or traditional formulation.

Detailed description

The randomized, double-blind, cross-over study was conducted under the supervision of physician on a group of 10 healthy subjects. The volunteers received 1g of vitamin C in a traditional formulation (powder in capsules), and after 14 days of a washout period 1 gram of liposomal formulation (powder in capsules). Venous blood was collected from each participant of the study immediately before the administration of a studied substance and 30 minutes, 1 hour, 2 hours, 3 hours, 4 hours, 6 hours, 8 hours, 10 hours, 24 hours post the administration.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTLiposomal Vitamin C1000 mg of ascorbic acid in liposomal formulation
DIETARY_SUPPLEMENTTraditional Vitamin C1000 mg of ascorbic acid in traditional formulation

Timeline

Start date
2022-02-28
Primary completion
2022-06-09
Completion
2022-06-09
First posted
2023-05-06
Last updated
2024-08-01

Locations

1 site across 1 country: Poland

Source: ClinicalTrials.gov record NCT05843617. Inclusion in this directory is not an endorsement.