Trials / Completed
CompletedNCT06949592
Oral Bioavailability of the Phenolic Compounds in a Melissa Supplement
Evaluation of Oral Bioavailability of the Phenolic Compounds in a Melissa Supplement: Double-blind, Randomized, Crossover Study
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 10 (actual)
- Sponsor
- Fytexia · Industry
- Sex
- All
- Age
- 18 Years – 60 Years
- Healthy volunteers
- Accepted
Summary
The objective of this study is to identify phenolic compound biomarkers of the intake of a mixture of Melissa officinalis extract, acerola extract and vitamin B5. This will be done through the study of their bioavailability and nutrikinetics by measuring their plasma concentrations and urinary excretion over 24h by means of high-performance liquid chromatography coupled with tandem mass spectrometry (HPLC-MS/MS). The study follows a cross-over, double-blind, randomized and placebo control design on 10 healthy subjects
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Placebo | Intake of 400 mg placebo (maltodextrin; encapsulated) in the morning (09:00) |
| DIETARY_SUPPLEMENT | M_ML | Intake of 400 mg M\_ML (encapsulated) in the morning (09:00) |
| DIETARY_SUPPLEMENT | M_ML | Intake of 400 mg M\_ML (encapsulated) in the evening (19:00) |
Timeline
- Start date
- 2025-04-30
- Primary completion
- 2025-06-12
- Completion
- 2025-06-12
- First posted
- 2025-04-29
- Last updated
- 2025-06-15
Locations
1 site across 1 country: Spain
Source: ClinicalTrials.gov record NCT06949592. Inclusion in this directory is not an endorsement.