Effects of Urolithin A Supplementation on Glucose Metabolism in Healthy Adults 55 = Years Old: A Randomized Triple-Masked Controlled Clinical Trial - Trial NCT06274749
Access comprehensive clinical trial information for NCT06274749 through Pure Global AI's free database. This phase not specified trial is sponsored by National Institute on Aging (NIA) and is currently Recruiting. The study focuses on Healthy Volunteer. Target enrollment is 180 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.
Study Focus
Sponsor & Location
National Institute on Aging (NIA)
National Institutes of Health Clinical Center (CC)
Timeline & Enrollment
N/A
Apr 01, 2024
Mar 31, 2027
Primary Outcome
To determine if urolithin A supplementation will influence insulin secretion in response to oral glucose at 4 and 8 weeks after supplementation.
Summary
Background:
 
 As people age, the cells in the pancreas that produce insulin begin to release less of this
 hormone, and levels of blood glucose (sugar) rise. This can lead to illnesses such as
 diabetes. Urolithin A (UA) is a natural nutritional supplement that may improve how the body
 controls blood glucose.
 
 Objective:
 
 To learn if UA improves levels of insulin and other hormones that help control blood glucose.
 
 Eligibility:
 
 People aged 55 years and older with a body mass index of 27 or higher.
 
 Design:
 
 Participants will have 6 clinic visits over 8 weeks.
 
 Participants will be screened. They will have a physical exam with blood and urine tests and
 a test of their heart function.
 
 UA gelcaps are taken by mouth every morning at home. Half of participants will take UA. The
 other half will take a placebo. The placebo looks like the study drug but does not contain
 any medicine. Participants will not know which they are taking.
 
 Participants will have tests during the study including:
 
 Oral glucose tolerance: Participants will drink a sweet liquid. Blood will be drawn at
 intervals over the next 3 hours.
 
 Continuous glucose monitor: A sensor with a needle that goes just under the skin will be
 placed on the upper arm. Participants will wear this sensor throughout the study.
 
 Exercise. Participants will walk on a treadmill while their heart rate, hearth rhythm, and
 blood pressure are monitored. They will walk in a hallway at normal and fast paces.
 
 Imaging scans of the thigh; scans of the brain are optional....
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT06274749
Non-Device Trial

