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Clinical Trials in China / NCT06907329
Recruiting Not applicable

The Impact of Nicotinamide Mononucleotide Sustained-release Tablets on Immunosenescence and Metablism in Middle-aged and Elderly Individuals With Metabolic Disorders.

NCT06907329 · tracked via the Priya Life Science China tracker
Sponsor
Qing Su
Phase
Not applicable
Started
2025-06-05
Last updated
2025-07-08

Condition(s) studied

ImmunosenescenceMetabolism

Investigational drug(s) / intervention(s)

NMNPlacebo

NMN: NMN SR tablets(1000mg/tablets) , 1 tablet daily before breakfast

Placebo: Matching Placebo (tablets) once daily before breakfast

Study summary

The ageing of our country is increasing and the ageing of the population has led to a significant increase in aging related diseases. During the aging process of the organism, cellular senescence can occur in all systems of the body, of which the senescence of the immune system is called immunosenescence. Some studies have shown that metabolic disorders can also trigger aging. This study investigated the effect of nicotinamide mononucleotide (NMN) supplementation on immunosenescence in middle-aged and elderly people through a placebo-controlled long-range clinical trail, aiming to provide a new method to improve immunosenescence. The effects of NMN supplementation on glucose and lipid metabolic indexes, body composition and telomere length of peripheral blood cells are also investigated, which may open up new ideas for the prevention and treatment of glucose and lipid metabolic diseases.

Eligibility

Sex
ALL
Min age
50 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: 1. Age 50-70 years with overweight or obesity (BMI 24kg/m2); 2. At least one of the following three: metabolism-related fatty liver disease (diagnosed by ultrasound); pre-diabetes; type 2 diabetes mellitus with HbA1c \<7% without glucose-lowering drug therapy; 3. Agreed to participate in the trial and could adhere to the follow-up and visit the hospital on their own; signed the informed consent form. Exclusion Criteria: 1. Patients with tumours; 2. Patients with autoimmune diseases (excluding Hashimoto's thyroiditis); 3. Severe cardiovascular disease or cardiac insufficiency; 4. Systolic blood pressure \> 160 mmHg or diastolic blood pressure \> 100 mmHg; 5. Chronic obstructive pulmonary disease; 6. Chronic active hepatitis or cirrhosis; 7. Chronic renal insufficiency; 8. Stroke patients 9. Severe haematological diseases; 10. Infectious diseases; 11. Mental illness; 12. Other conditions that, in the opinion of the investigator, may affect the results of the study; 13. Those who have used NMN or other anti-aging agents within six months. 14. Premenopausal woman 15. ALT, AST values are more than three times higher than the upper limit of the normal reference range

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Xin Hua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine Shanghai China Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06907329 on ClinicalTrials.gov ↗ ← All trials in China