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Anti-aging and Anti-oxidant Efficacy Evaluation of the MelaGene

Anti-aging and Anti-oxidant Efficacy Evaluation of the MelaGene

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05191056
Enrollment
51
Registered
2022-01-13
Start date
2021-09-15
Completion date
2022-02-28
Last updated
2022-03-31

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

Conditions

Aging, Antioxidative Stress

Brief summary

The primary purpose of the present study is to evaluate the effects of MelaGene on anti-aging and anti-oxidant.

Interventions

DIETARY_SUPPLEMENTPlacebo drink

consume 1 bottle per day for 8 weeks

DIETARY_SUPPLEMENTMelaGene drink

consume 1 bottle per day for 8 weeks

Sponsors

TCI Co., Ltd.
Lead SponsorINDUSTRY

Study design

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

Eligibility

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

Inclusion criteria

* 30 to 65-year-old; * Must read and sign the informed consent form before the experiment; * People who are willing to cooperate with contraception during the trial period; * Do not change lifestyle and eating habits arbitrarily during the trial period; * Do not take supplementary foods and health supplements with the same efficacy two weeks before and during the test; * If any adverse reaction occurs during the experiment, subjects should be notified the researcher immediately.

Exclusion criteria

* Subject who is not willing to participate in this study; * Vegetarians; * People with a history of organ transplantation, epilepsy or convulsions, liver and kidney disease, malignant tumors, endocrine diseases, mental illness, alcohol or drug abuse, and other major organic diseases (according to medical history); * Participate in other clinical trials related to antioxidants and anti-aging four weeks before and during the test; * People with a history of dyspepsia would affect the absorption of the test product; * Allergic to the components of the test product; * Pregnant or breast-feeding women; * Take anti-oxidant supplements; * Undergoing hormone replacement therapy.

Design outcomes

Primary

MeasureTime frameDescription
The change of blood lipid (Triglyceride, total cholestrol, HDL-C, LDL-C)Days 1, 28, and 56Venous blood is sampled to measure concentrations of blood lipid (Triglyceride, total cholestrol, HDL-C, LDL-C)
The change of cardiovascular enduranceDays 1, 28, and 56Step test is designed to assess cardiovascular endurance
The change of blood antioxidants(f-Thiols, t-GSH, GST-RBC, SOD, Total Anit-oxidative Capicity)Days 1, 28, and 56Venous blood is sampled to measure concentrations of blood antioxidants(f-Thiols, t-GSH, GST-RBC, SOD, Total Anit-oxidative Capicity)
The change of ALT and ASTDays 1, 28, and 56Venous blood is sampled to measure concentrations of ALT and AST
The change of MDADays 1, 28, and 56Venous blood is sampled to measure concentrations of MDA
The change of anti-aging gene expressionDays 1, 28, and 56Venous blood is sampled to measure expression of anti-aging gene

Secondary

MeasureTime frameDescription
The change of continuous attention testDays 1, 28, and 56Continuous attention test is designed to assess cognitive performance
The change of fatigue conditionDays 1, 28, and 56BFI-Taiwan Form is collected to assess fatigue condition

Countries

Taiwan

Outcome results

None listed

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