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
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Liposomal Vitamin C | 1000 mg of ascorbic acid in liposomal formulation |
| DIETARY_SUPPLEMENT | Traditional Vitamin C | 1000 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.