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A human trial on the effects of Kinetic Pills Pro dietary supplement on multidimensional health indicators in healthy populations

A human trial on the effects of Kinetic Pills Pro dietary supplement on multidimensional health indicators in healthy populations

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108127
Enrollment
Unknown
Registered
2025-08-25
Start date
2025-07-22
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

None listed

Interventions

Test Group:Take one capsule daily with or without food for 60 consecutive days

Sponsors

Central Hospital of Fengxian District, Shanghai
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Age between 35-60 years, with equal number of males and females (20 subjects aged 35-45 and 20 subjects aged 45-60); (2) Able to read Chinese and accurately understand the trial process, voluntarily participated in the trial and signed the informed consent form for the research; (3) Able to cooperate with and attend follow-up visits as required, promptly report personal health status or any changes in medication, adverse reaction symptoms, and able to comply with research requirements and schedule arrangements.

Exclusion criteria

Exclusion criteria: (1) Patients with severe diseases of the heart, liver, kidney, hematopoietic system, etc.; (2) Patients with severe mental illness or cognitive impairment who cannot make independent decisions; (3) Possible vascular, traumatic, or medically-induced decline in motor function; (4) Consumption of products related to the subject's function (such as ergothioneine, hyaluronic acid, spermidine, sialic acid, bird's nest, etc.) within the past 2 weeks; (5) Use of any antibiotics or alcohol abuse in the past 1 month; (6) Patients who have participated in other drug clinical trials in the past 1 month; (7) Pregnant, planning to become pregnant, or lactating women; (8) Patients who may be allergic to the test samples or their ingredients; (9) Individuals assessed by the investigator as unsuitable for participation in the trial.

Design outcomes

Primary

MeasureTime frame
Facial image acquisition and analysis (VISIA CR5): Image acquisition analyzes the area and number of crow's feet wrinkles;Skin Color ITA° Value (VISIA CR5);Percentage of facial pigmented spots (VISIA CR5): Facial Pigmented Spots;Skin Elasticity (Cutometer dual MPA580);Skin Stratum Corneum Moisture Content Value (Corneometer CM825);Observation Index Scoring of Scalp Hair Microenvironment and Hair Quality: Itching, Oiliness, Dandruff Severity, and Hair Loss Situation;Dermatoscopy (MoleMaxHD): Analysis of total hair count, hair density;Blood pressure levels;Body composition analysis (height, weight, muscle mass, skeletal muscle, body fat percentage, waist circumference (Waist cir.), visceral fat area (VFA), basal metabolic rate (BMR));Fatigue Scale-14 Score (FS-14);Brain Test: Instant Memory, Concentration, and Reaction Test (completed using the Wind-style Brain Training mini-program);Objective sleep assessment: Using the Huawei Band 9 to assess subjects' sleep: sleep onset time, wake-up time, number of awakenings, awake duration, deep sleep, light sleep, rapid eye movement (REM), total sleep time;Pittsburgh Sleep Quality Index (PSQI) score;DNA Methylation Age Test;

Secondary

MeasureTime frame
Mental status, sleep, diet, urination and defecation are the main clinical symptoms.;Blood routine, urine routine, liver and kidney function, blood pregnancy test;

Countries

China

Contacts

Public ContactZhu Haiying

Central Hospital of Fengxian District, Shanghai

zhuhaiying751112@163.com+86 21 5742 0702

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026