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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.

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NCT06274749
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dietary supplement
Trial Details
ClinicalTrials.gov โ€ข NCT06274749
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Effects of Urolithin A Supplementation on Glucose Metabolism in Healthy Adults 55 = Years Old: A Randomized Triple-Masked Controlled Clinical Trial
The Effects of Urolithin A Supplementation on Glucose Metabolism in Healthy Adults = 55 Years Old. A Randomized Triple-Masked Controlled Clinical Trial

Study Focus

Healthy Volunteer

Urolithin A

Interventional

dietary supplement

Sponsor & Location

National Institute on Aging (NIA)

National Institutes of Health Clinical Center (CC)

Baltimore, United States of America

Timeline & Enrollment

N/A

Apr 01, 2024

Mar 31, 2027

180 participants

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

Healthy person accompanying sick person
Routine general health check-up of armed forces
Persons encountering health services in other circumstances
Persons encountering health services in other circumstances
Person encountering health services in unspecified circumstances

Data Source

ClinicalTrials.gov

NCT06274749

Non-Device Trial