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
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Acerola Juice Powder 1200 mg/day | 4 capsules per day, each capsule containing 300mg of Acerola and 100 mg of maltodextrin |
| DIETARY_SUPPLEMENT | Acerola Juice Powder 600 mg/day | 4 capsules/day, each capsule containing 150 mg of Acerola and 250 mg of Maltodextrin |
| OTHER | Placebo | 4 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.