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Efficacy Determination of microemulsion serum from fermented riceberry bran THE TREATMENT SERUM

Efficacy Determination of microemulsion serum from fermented riceberry bran THE TREATMENT SERUM

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20220215005
Enrollment
33
Registered
2022-02-15
Start date
2019-07-09
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 female volunteers age between 20-55 years old Skin hydration, wrinkles, skin elasticity, skin lightening, Transepidermal water loss

Interventions

Treatment at facial skin for 8 weeks [ before treatment with the product [baseline]]&#44
2 week&#44
4 week&#44
6 week and 8 week]
Experimental Other
THE TREATMENT SERUM

Sponsors

Mr. Jirasit Inthorn, Pibulsongkram Rajabhat University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Healthy female age between 20-55 years old 2. All skin types 3. Having clearly visible wrinkle at eye corner [ crow's feet] or forehead 4. Having Fitzpatrick skin type II-V 5. Having experience using a counter brand facial skin care 6. No wound, scar or any dermatological disorder on face 7. No smoking, alcoholic drinking or addiction to any narcotic substances history 8. No allergic history to any ingredient in commercially available anti-wrinkle products or cosmetics in the market 9. Willing to participate in the study after being informed objective, methodology, possible risk and result, and be able to follow the study protocol during the 8-week study period 10. Be able to read, communicate and write Thai language

Exclusion criteria

Exclusion criteria: 1. Having a history of hyperallergic reaction 2. Having a history of skin eczema psoriasis within 6 months before enter the study 3. Having a history of using steroid antibiotic NSAIDs and antihistamine within 3 days before enter the study 4. Having a history of using any topical medicine on the face in the last 3 weeks before enter the study 5. Having underlying disease and continuous taking or applying medicine for facial treatment 6. History of major operation within 1 year 7. History of skin cancer within 1 year 8. Having pregnancy or lactation 9. Having wound and scar around study-evaluating face area 10. Having history of participating in other clinical study within 3 months before enrollment in this study 11. Having allergic history of rice or rice extract cosmetic product

Design outcomes

Primary

MeasureTime frame
Skin moisture 8 weeks Corneometer,Skin roughness and wrinkles 8 weeks Primos,Skin elasticity 8 weeks Cutometer,Skin lightening effect 8 weeks Mexameter,Transepidermal Water Loss 8 weeks Tewameter, Crow's feet area. 8 weeks Digital photograph [ Canon EOS Rebel T5i 700D]

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.th6655968801

Outcome results

None listed

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