Anti-aging and Anti-oxidant Efficacy Evaluation of the MelaGene (NCT05191056) | Clinical Trial Compass
CompletedNot Applicable
Anti-aging and Anti-oxidant Efficacy Evaluation of the MelaGene
Taiwan51 participantsStarted 2021-09-15
Plain-language summary
The primary purpose of the present study is to evaluate the effects of MelaGene on anti-aging and anti-oxidant.
Who can participate
Age range
30 Years – 65 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
The change of blood lipid (Triglyceride, total cholestrol, HDL-C, LDL-C)
Timeframe: Days 1, 28, and 56
2
The change of ALT and AST
Timeframe: Days 1, 28, and 56
3
The change of MDA
Timeframe: Days 1, 28, and 56
4
The change of blood antioxidants(f-Thiols, t-GSH, GST-RBC, SOD, Total Anit-oxidative Capicity)