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Efficacy Evaluation of Pitaya Ovule Extract on Skin

Efficacy Evaluation of Pitaya Ovule Extract on Skin

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05311020
Enrollment
50
Registered
2022-04-05
Start date
2022-10-19
Completion date
2023-01-16
Last updated
2023-02-09

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 Pitaya Ovule Extract on skin

Interventions

DIETARY_SUPPLEMENTPlacebo drink

consume 1 bottle per day

DIETARY_SUPPLEMENTPitaya Ovule 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

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 Matrix metalloproteinases (MMP-2, MMP-9) of bloodChange from Baseline MMPs at 8 weeksVenous blood was sampled to measure MMPs
The change of skin textureChange from Baseline skin texture at 8 weeksIRV skin analyzer was utilized to measure skin texture. Units: arbitrary units
The change of skin poresChange from Baseline skin pores at 8 weeksIRV skin analyzer was utilized to measure skin pores. Units: arbitrary units
The change of skin toneChange from Baseline skin tone at 8 weeksIRV skin analyzer was utilized to measure skin tone. 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 RAGE (receptor for advanced glycation end products) of bloodChange from Baseline RAGE at 8 weeksVenous blood was sampled to measure RAGE
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 skin elasticityChange from Baseline skin elasticity at 8 weeksCutometer® Dual MPA580 was utilized to measure skin elasticity. Units: arbitrary units
The change of skin collagen densityChange from Baseline skin collagen density at 8 weeksDermaLab® Combo Ultrasound module was utilized to measure skin collagen density. Units: arbitrary units
The change of skin wrinklesChange from Baseline skin wrinkles at 8 weeksIRV skin analyzer was utilized to measure skin wrinkles. Units: arbitrary units

Secondary

MeasureTime frameDescription
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 glucose levelChange from Baseline fasting blood glucose level at 8 weeksVenous blood was sampled to measure fasting blood glucose level
Change from Baseline insulin level at 8 weeksChange from Baseline insulin level at 8 weeksVenous blood was sampled to measure insulin 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 liver function biomarkers (AST, ALT) of bloodChange from Baseline liver function biomarkers at 8 weeksVenous blood was sampled to measure liver function biomarkers

Countries

Taiwan

Outcome results

None listed

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