The Efficacy of Topical Serum X for Skin Brightening
1 other identifier
interventional
34
1 country
1
Brief Summary
This study is conducted to evaluate the effectiveness of topical serum X containing arbutin and glutathione for skin brightening. The study duration is 12 weeks and the skin assessment will be carried out at baseline, week 4, 8 and week 12.The main questions this study aims to answer are:
- 1.The skin brightening effect of the product on facial skin.
- 2.To observe any adverse effect occurrence with the usage of the product.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable healthy
Started Sep 2022
Typical duration for not_applicable healthy
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2022
CompletedFirst Submitted
Initial submission to the registry
January 11, 2023
CompletedFirst Posted
Study publicly available on registry
January 23, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 31, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2023
CompletedNovember 29, 2023
November 1, 2023
9 months
January 11, 2023
November 27, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Changes in skin tone from baseline and at week 4, week 8, and week 12 after usage of serum X.
Skin tone will be assessed using JANUS III skin analyzer
Baseline and at week 4, week 8, and week 12
Adverse effect after using serum X
Based on adverse effect occurrence on participants that occur during study period (12 weeks
Week 12
Study Arms (1)
Serum X
EXPERIMENTALParticipants will used serum X twice daily for 12 weeks
Interventions
Eligibility Criteria
You may qualify if:
- Malaysia citizen
- Male and female (age 18-30 years old)
You may not qualify if:
- Participant with severe acne skin condition
- Participant who is taking isotretinoin, immunocompromised patients and received laser and light treatment within the last three months
- Participant who undergo whitening or cosmetic treatments such as botox and dermal fillers within the previous six month
- Participant with a history of facial surgery such as facelift or nose reshaping
- Participant with history of allergies to any ingredient in the study product
- Participant who is pregnant or plan to get pregnant
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ungku Shahrin Medical Aesthetic Research & Innovation (USMARI) Centre
Petaling Jaya, Selangor, 47810, Malaysia
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 11, 2023
First Posted
January 23, 2023
Study Start
September 1, 2022
Primary Completion
May 31, 2023
Study Completion
September 1, 2023
Last Updated
November 29, 2023
Record last verified: 2023-11
Data Sharing
- IPD Sharing
- Will not share