UthPeak NMNH for Safety and Tolerability in Healthy Adults
NMNH
+ Placebo
Other Study
Summary
Study start date: July 8, 2024
Actual date on which the first participant was enrolled.This study investigates the safety and how the body processes a compound called UthPeak NMNH, which is a form of nicotinamide mononucleotide. It involves 80 healthy adults who meet specific health criteria. The aim is to understand if different doses of NMNH, taken orally over 90 days, are safe and well-tolerated. This research is important as it could provide insights into how NMNH might support health and well-being by evaluating changes in NAD+ levels, which are linked to energy production and cellular health. Participants are divided into four groups, each receiving either a placebo or different doses of NMNH (125 mg, 250 mg, or 500 mg). They take the supplement daily and have their NAD+ levels, physical abilities, and quality of life assessed at the start, middle, and end of the study. Blood samples are collected at various times after the first dose to measure NAD+ levels, focusing on how the body absorbs and processes the supplement. Regular health checks and monitoring for side effects ensure participant safety.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.80 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 40 to 65 Years
Range of ages for which participants are eligible to join.Healthy volunteers 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.4 intervention groups are designated in this study
25% chance of being blinded to the placebo group
Treatment Groups
Group I
ExperimentalGroup II
ExperimentalGroup III
ExperimentalGroup IV
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 2 locations
Vinayaka Mission's Medical College and Hospital
Kāraikāl, India