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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05694182
Other study ID # UMRAMREC003-22
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date December 1, 2022
Est. completion date December 1, 2023

Study information

Verified date August 2023
Source Ungku Shahrin Medical Aesthetic Research & Innovation (USMARI) Centre
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 15
Est. completion date December 1, 2023
Est. primary completion date June 30, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria: - Malaysian citizen - Male and female (age 20-60 years old) Exclusion Criteria: - Participant who taking any dietary supplements for the past 4 weeks which can affect the study results - Participant who are on contraceptive pills for the past 3 months - Participant who undergo cosmetics treatments such as botox, filler and laser and light treatment within the last 3 months - Pregnant or plans to get pregnant and breastfeeding women

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Other: Oral superfruits supplement
The supplement contain superfruits that are beneficial for human health

Locations

Country Name City State
Malaysia Ungku Shahrin Medical Aesthetic Research & Innovation (USMARI) Centre Petaling Jaya Selangor

Sponsors (1)

Lead Sponsor Collaborator
Ungku Shahrin Medical Aesthetic Research & Innovation (USMARI) Centre

Country where clinical trial is conducted

Malaysia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in skin tone from baseline and at week 2, week 6 and week 12 after consumption of the superfruits supplement Skin tone will be assessed using JANUS III skin analyzer Baseline, week 2, week 6 and week 12
Primary Changes in skin wrinkles from baseline and at week 2, week 6 and week 12 after consumption of the superfruits supplement Skin wrinkles will be assessed using JANUS III skin analyzer and Wrinkle Severity Rating Scale (WSRS). For WSRS, dermatologists will evaluate participants' wrinkles based on 5-point photonumeric rating scale that will objectively evaluate the severity of crow's feet at rest (static) and with a smiling expression (dynamic). The scale scores are 0 for no wrinkles, 1 for very fine wrinkles, 2 for fine wrinkles, 3 for moderate wrinkles, and 4 for severe wrinkles. Baseline, week 2, week 6 and week 12
Primary Adverse effect after consumption of the superfruits supplement Based on adverse effect occurrence on participants that occur during study period (12 weeks) Week 12
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