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Efficacy Determination of Skin Lightening Body Lotions SWBL4 and FBL65

Efficacy Determination of Skin Lightening Body Lotions SWBL4 and FBL65

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20190617001
Enrollment
Unknown
Registered
2019-06-17
Start date
2018-04-23
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Thai female subjects aged between 25&#45

Interventions

33 Thai female subjects with age in range of 25&#45
60 years old were selected according to predefined inclusion and exclusion criteria
Other
Skin lightening body lotion test

Sponsors

Unilever thai services co. ltd
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Healthy volunteers with an age in a range of 25-60 year old 2. Having dark skin and one homogenous 3x3 cm area on each lateral forearm for product use, clinical and instrumental evaluation 3. Having little or no hair on the lateral forearm 4. Having experience using counter brand 5.No history of allergies against any components of trial products or lightening cosmetics 6. Be able to use only provided products and no other similar products during the test period 7. No functional supplements with improving skin condition or no treatment prior to the clinical test for 1 month 8. Agree to refrain from using any cream, lotions, moisturizers, sunscreens, bath addictive or any other skin products on the forearm for the during of washout phase and study period 9. Agree to refrain from using depilatory cream or shaving thr forearm during the course of study 10. Agreement on refraining from swimming, tanning and sunbathing during the cause of the study 11. Be able to read, write and communicate well in Thai 12. Be able to follow the study protocol 13. Understanding and willing to give consent of the volunteer

Exclusion criteria

Exclusion criteria: 1. Regular use of the cream, lotions, moisturizers, sunscreens, bath additives or any other skin products on the forearms 2. Having big skin color difference between two forearms 3. Having history of any type of cancer in the last five years 4. Having other erythema, sunburn, cuts and/or abrasions on the forearms 5. Taking medication which the investigator believes may influence the interpretation of the data, such as photosensitizing drugs or chronic users of corticiosteriods or non-steroidial anti-inflammatoies (Ibruprofen or aspirins) 6. Having extreamly dry skin 7. Participating in any other study concurrently 8. Participated in the study in which the lateral forearms were used as a test site within 3 months prior to the start of this study 9. Current use of having a skin lightening or alpha hydroxyl acid product on the forearm within the last 6 months 10. Current use or having usr the hormonal contractive method, e.g pill, injection, implant, with the last 6 months 11. Having any of the following conditions or factor that investigator belives may effect the response of the skin or the interpretation of the test results, including, but not limited to, diabets, pregnancy, lactation, vascular disease, hepatitis, eczema, psoriasis and acne 12. History of major operation within 1 year 13. Working as a fieldworker or salesperson

Design outcomes

Primary

MeasureTime frame
Quantification of the lightening effect week 0, 1, 2, 4 Chromameter,Erythema Value ane melanin index week 0, 1, 2, 4 Mexameter,Visual evaluation the product effect week 0, 1, 2, 4 photography,Consumer eslf-assessment week 1, 2, 4 Questionnaire form

Secondary

MeasureTime frame
N/A N/A N/A

Countries

Thailand

Contacts

Public ContactNeti Waranuch

Cosmetics and natural products research center, Faculty of Pharmaceutical Sciences, NU

cosnat@nu.ac.th+6655968801

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026