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Study identifier: NCT07265323 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Effect of Physiologic Insulin Administration on Insulin Sensitivity and Cognition

Condition: Alzheimer s Disease · Alzheimer Blood Biomarkers · Insulin Sensitivity  ·  Sponsor: Pennington Biomedical Research Center

PhaseNA
Planned participants8
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this clinical trial is to determine if a weekly delivery of insulin at short intervals lasting up to 2 hours can improve insulin sensitivity and cognition in adults with Alzheimer's Disease. It will also provide information about the safety and feasibility of this intervention. The main questions it aims to answer are: Does the intervention improve insulin sensitivity (how the body uses glucose)? Does the intervention improve cognition, measured by the Montreal Cognitive Assessment (MoCA) and the Revised Memory and Behavior Problems Checklist (RMBPC)? What changes occur in brain glucose uptake (FDG-PET)? Participants will: Receive the intervention once a week for 6 months, with each session lasting up to 2 hours Complete cognitive assessments. Adverse events will be assessed throughout the study.

This description comes directly from the study's public registry record.

Talk to the study team

Tim Gilbert, M.D.  ·  2257632584  ·  Tim.Gilbert@pbrc.edu

Candida Rebello, Ph.D.  ·  2257633159  ·  Candida.Rebello@pbrc.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Pennington Biomedical Research CenterBaton Rouge, Louisiana, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07265323