Clinical Trials Directory

Trials / Completed

CompletedNCT05694182

The Safety and Efficacy of an Oral Superfruits Supplement

The Safety and Efficacy of an Oral Superfruits Supplement for Skin Brightening and Wrinkle Reduction

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
15 (actual)
Sponsor
USMARI Research & Innovation Centre · Industry
Sex
All
Age
20 Years – 60 Years
Healthy volunteers
Accepted

Summary

This study is conducted to evaluate the safety and effectiveness of an oral superfruits supplement for skin brightening and wrinkle reduction. Superfruits are reported to have high bioactive compounds with beneficial effects on human health. The study duration is 12 weeks and the skin assessment will be carried out at baseline, week 2, week 6 and week 12. The participants will consume the supplement for 6 weeks and at week 12, final skin assessment will be conducted. The main questions this study aims to answer are: 1. The skin brightening effect of the oral superfruits supplement. 2. The effect of the oral superfruits supplement on wrinkle reduction. 3. To observe any adverse effect occurrence with the consumption of the oral superfruits supplement.

Conditions

Interventions

TypeNameDescription
OTHEROther: Oral superfruits supplementThe supplement contain superfruits that are beneficial for human health

Timeline

Start date
2022-12-01
Primary completion
2023-06-30
Completion
2023-12-01
First posted
2023-01-23
Last updated
2025-03-28

Locations

1 site across 1 country: Malaysia

Source: ClinicalTrials.gov record NCT05694182. Inclusion in this directory is not an endorsement.