Nicotinamide Mononucleotide for Immunosenescence in Middle-aged and Elderly with Metabolic Disorders
NMN
+ Placebo
Other Study
Summary
Study start date: June 5, 2025
Actual date on which the first participant was enrolled.This study is exploring the effects of a supplement called Nicotinamide Mononucleotide (NMN) on the immune system and metabolism of older adults. Specifically, it targets those aged 50 to 70 who have metabolic disorders, aiming to see if this supplement can improve immune function and metabolic health. The importance of this study lies in its potential to enhance the quality of life for middle-aged and elderly individuals by addressing age-related declines in immunity and metabolic function. Participants in the study will take one NMN sustained-release tablet or a placebo daily before breakfast for 26 weeks. The researchers will monitor participants through visits at months 1, 3, and 6. The main focus is on measuring specific immune cells in the blood to see the impact of NMN. Additionally, the study will look at secondary factors such as liver fat, body composition, blood sugar levels, and overall fitness. Safety will be evaluated by checking routine blood and urine tests, and assessing liver and kidney function.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.126 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Other Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 50 to 70 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
50% chance of being blinded to the placebo group
Treatment Groups
Group I
ExperimentalGroup II
PlaceboStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Xin Hua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
Shanghai, ChinaOpen Xin Hua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine in Google Maps