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Efficacy Determination of AdeYa Jellyfish Hydration & Lightening

Efficacy Determination of AdeYa Jellyfish Hydration & Lightening

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20220208005
Enrollment
33
Registered
2022-02-08
Start date
2020-11-09
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 male or female volunteers (30-60 years old) Skin hydration, skin lightening

Interventions

Corneometer, Chromameter, Mexameter and Visia CR are used to assess skin conditions and skin color before using the product (1st time) and after using the product for 2 weeks (2nd time), 4 weeks (3rd)
Experimental Other
AdeYa Jellyfish Hydration &amp
Lightening

Sponsors

Adeya Marketing Company Limited
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Healthy male or female aged 30-60 years 2. Having any type of facial skin (normal, dry, oily or combination) 3. Having clear visible melasma, freckles and dark spots on facial skin*. 4. Having history of using counter brand facial skin care 5. Be able to read, communicate and writing Thai language 6. Willing to stop using other anti-melasma, anti-freckle and anti-dark spots products. Other routine skin care products without mentioned properties were allowed. Changing any skin care product during the study period was not acceptable. 7. Willing to participate in the study after be informed the study objectives, methodology, possible risks and results. Note: *The difference on Maxameter melanin index between blemish area and normal area was 20-120

Exclusion criteria

Exclusion criteria: 1. Having history of hyperallergic reaction to the composition in anti-melasma, anti-freckle and anti-dark spots products 2. History of skin eczema or psoriasis at any part of body within 6 months before entering the study 3. History of using steroid, antibiotic, oral Tranexamic acid, NSAIDs and antihistamine within 3 days before entering the study 4. History of using topical medicine on facial area within 3 weeks before entering the study 5. Having chronic diseases and continuous taking medicines or applying topical drug for facial skin treatment 6. History of major operation within 1 year before entering the study. 7. History of skin cancer at any parts of body within 1 year before entering the study. 8. Pregnancy or lactation 9. Having wound or scar on the evaluation areas of the face 10. History of regular smoker or regular drinking alcohol (Definitions: 1. Regular smoker means smoking everyday at least 1 cigarette per day. 2. Regular drinking means drinking alcohol everyday at least 1 cup or around 250 ml per day) 11. History of participating or ongoing testing in other clinical studies of CosNat which were tested on the face within last 3 months (since the last day of the previous study to the volunteer selection date of this study)

Design outcomes

Primary

MeasureTime frame
Skin color, Facial skin measurement in 3D 8 weeks The photograph of facial area by Visia CR,Skin hydration 8 weeks Measuring by Corneometer,Skin color 8 weeks Measuring by Chromameter,Melanin and erythema index of skin 8 weeks Measuring by Mexameter

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.th055968801

Outcome results

None listed

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