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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05691413
Other study ID # UMRAMREC004-22
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 1, 2022
Est. completion date September 30, 2023

Study information

Verified date November 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 facial cleanser X containing combination of olive oil, virgin coconut oil, butylene glycol and hyaluronic acid on skin hydration and skin elasticity. The study duration is 5 weeks and the skin assessment will be carried out at baseline, week 3 and week 5.The main questions this study aims to answer are: 1. The effect of product on skin hydration. 2. The effect of product on skin elasticity. 3. To observe any adverse effect occurrence with the usage of the product.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date September 30, 2023
Est. primary completion date August 31, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 35 Years to 55 Years
Eligibility Inclusion Criteria: - Malaysia citizen - Male and female (age 35-55 years old) Exclusion Criteria: - Participants who have acne which require medical treatment. - Participants taking isotretinoin - Participants who had undergo any cosmetic procedures such as laser & light treatment, botulinum toxin A injections and chemical peeling for the past 3 months - Participants who are immunocompromised - Participants with history of facial surgery

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Other: Product X facial cleanser
Product X facial cleanser contain olive oil, virgin coconut oil, butylene glycol and hyaluronic acid

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 Change in skin hydration from baseline and at week 3 and 5 after using facial cleanser X Skin hydration will be assessed using JANUS III skin analyzer Baseline, week 3 and week 5
Primary Change in skin elasticity from baseline and at week 3 and 5 after using facial cleanser X Skin elasticity will be assessed using JANUS III skin analyzer Baseline, week 3 and week 5
Primary Adverse effect after using facial cleanser X Based on adverse effect occurrence on participants that occur during study period (5 weeks) Week 5
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