Clinical Trials Directory

Trials / Completed

CompletedNCT07229131

Effect of an Oral Acerola Juice Powder on Skin Beauty Parameters in Women Exposed to Environmental Stresses

Effect of an Oral Acerola Juice Powder on Skin Beauty Parameters in Women Exposed to Environmental Stresses: A Double-blind, Randomised, Placebo-controlled Study.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
108 (actual)
Sponsor
Diana SAS · Industry
Sex
Female
Age
30 Years – 60 Years
Healthy volunteers
Not accepted

Summary

The study is being conducted to evaluate the efficacy and the safety of an oral acerola-based product on skin ageing parameters.

Detailed description

The main objective of this study is to assess efficacy of the product on skin translucency after 84 days of product compared to a placebo. The study will also evaluate the effect of the product on different skin parameters (radiance, firmness, elasticity, skin barrier function, skin pH, blood flow) with different instruments. The quality of life and the improvement of skin properties will also be collected with questionnaires completed by the subjects. Finally, the safety of this product will be assessed by collecting all adverse events that might occur during the study.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTAcerola Juice Powder 1200 mg/day4 capsules per day, each capsule containing 300mg of Acerola and 100 mg of maltodextrin
DIETARY_SUPPLEMENTAcerola Juice Powder 600 mg/day4 capsules/day, each capsule containing 150 mg of Acerola and 250 mg of Maltodextrin
OTHERPlacebo4 capsules per day, each capsule containing 400 mg of maltodextrin

Timeline

Start date
2025-11-03
Primary completion
2026-02-13
Completion
2026-02-13
First posted
2025-11-14
Last updated
2026-02-18

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07229131. Inclusion in this directory is not an endorsement.