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Efficacy Evaluation of Wasabi Leaf Extract on Skin

Efficacy Evaluation of Wasabi (Wasabia Japonica) Leaf Extract on Skin

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05310994
Enrollment
50
Registered
2022-04-05
Start date
2022-03-28
Completion date
2022-07-31
Last updated
2022-09-29

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

Conditions

Skin Condition

Brief summary

To assess the efficacy of Wasabi Leaf Extract on skin

Interventions

DIETARY_SUPPLEMENTPlacebo drink

consume 1 bottle per day

DIETARY_SUPPLEMENTWasabi Leaf Extract Drink

consume 1 bottle per day

Sponsors

TCI Co., Ltd.
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
20 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* 20 to 65-year-old males or females * People with dull skin, pigmentation spots or acne-prone, acne scars * Acne severity assessment- Investigator's Global Assessment Scale (IGA) ≥ 2

Exclusion criteria

* Received medical cosmetic treatment (including cosmetic skin care, laser, fruit acid peeling, injection or plastic surgery, etc.) currently or within one month before the trial * Outdoor workers (exposed to the sun more than 5 hours a day) * People who are breastfeeding, pregnant or planning to become pregnant during the test (self-report) * People with heart, liver, kidney, endocrine and other major organic diseases (self-reported) * People who have undergone major surgery (according to medical history) * People who take drugs for a long time * People with mental illness * Students who are currently taking courses taught by the principal investigator of this trial

Design outcomes

Primary

MeasureTime frameDescription
The change of Insulin-Like Growth Factor-1 of bloodChange from Baseline IGF-1 at 8 weeksVenous blood was sampled to measure IGF-1
The change of transepidermal water lossChange from Baseline TEWL at 8 weeksTewameter® TM300 was utilized to measure transepidermal water loss (TEWL). Units: TEWL-values lower than 70 g/hm²
The change of L* (lightness) valuesChange from Baseline L* value at 8 weeksSpectrophotometer SCM-108 was utilized to measure skin L\* value. Units: arbitrary units
The change of a* (redness) valuesChange from Baseline a* value at 8 weeksSpectrophotometer SCM-108 was utilized to measure skin a\* value. Units: arbitrary units
The change of visible spotsChange from Baseline visible spots at 8 weeksVISIA Complexion Analysis System was utilized to measure skin spots. Units: arbitrary units
The change of skin red areaChange from Baseline skin red area at 8 weeksVISIA Complexion Analysis System was utilized to measure skin red area. Units: arbitrary units
The change of total antioxidant capacity of bloodChange from Baseline total antioxidant capacity at 8 weeksVenous blood was sampled to measure total antioxidant capacity
The change of Interleukin-6 of bloodChange from Baseline IL-6 at 8 weeksVenous blood was sampled to measure IL-6
The change of Interleukin-8 of bloodChange from Baseline IL-8 at 8 weeksVenous blood was sampled to measure IL-8
The change of skin melanin indexChange from Baseline skin melanin index at 8 weeksMexameter® MX18 was utilized to measure skin melanin index. Units: arbitrary Mexameter® units (0-999)
The change of skin erythema indexChange from Baseline skin erythema index at 8 weeksMexameter® MX18 was utilized to measure skin erythema index. Units: arbitrary Mexameter® units (0-999)
The change of skin sebum contentChange from Baseline skin sebum content at 8 weeksSebumeter® SM815 was utilized to measure skin sebum content. Units: Sebumeter® units from 0-350

Secondary

MeasureTime frameDescription
The change of UV spotsChange from Baseline UV spots at 8 weeksVISIA Complexion Analysis System was utilized to measure UV spots. Units: arbitrary units
The change of brown spotsChange from Baseline brown spots at 8 weeksVISIA Complexion Analysis System was utilized to measure brown spots. Units: arbitrary units
The change of Advanced glycation end products of bloodChange from Baseline AGEs at 8 weeksVenous blood was sampled to measure AGEs
The change of liver function biomarkers (AST, ALT) of bloodChange from Baseline liver function biomarkers at 8 weeksVenous blood was sampled to measure liver function biomarkers
The change of renal function biomarkers (creatinine, BUN) of bloodChange from Baseline renal function biomarkers at 8 weeksVenous blood was sampled to measure renal function biomarkers
The change of fasting blood glugose levelChange from Baseline fasting blood glugose level at 8 weeksVenous blood was sampled to measure fasting blood glugose level
The change of blood lipid profileChange from Baseline blood lipid profile at 8 weeksVenous blood was sampled to measure blood lipid profile (total cholesterol, HDL-C, LDL-C, triglyceride)
The change of skin hydrationChange from Baseline skin hydration at 8 weeksCorneometer® CM825 was utilized to measure skin hydration. Units: arbitrary

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026