Clinical Trials Directory

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

TypeNameDescription
DIETARY_SUPPLEMENTPlaceboIntake of 400 mg placebo (maltodextrin; encapsulated) in the morning (09:00)
DIETARY_SUPPLEMENTM_MLIntake of 400 mg M\_ML (encapsulated) in the morning (09:00)
DIETARY_SUPPLEMENTM_MLIntake 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.