Actively Recruiting

Early Phase 1
Age: 40Years - 65Years
All Genders
NCT06322212

Type 2 Diabetes and Blood Brain Barrier Improvement

Led by University of California, Los Angeles ยท Updated on 2026-03-13

52

Participants Needed

1

Research Sites

138 weeks

Total Duration

On this page

Sponsors

U

University of California, Los Angeles

Lead Sponsor

N

National Institute on Aging (NIA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The majority of T2DM adults show thiamine (vitamin B1) deficiency which may contribute to impaired function. This study will examine patients with T2DM through brain MRI scans, cognition assessments, blood tests, and questionnaires. Our goal is to see if a thiamine treatment (taking vitamin B1 capsules) can improve function. Patients will be asked to come to UCLA two times three months apart and each visit will last about 2.5-3 hours.

CONDITIONS

Official Title

Type 2 Diabetes and Blood Brain Barrier Improvement

Who Can Participate

Age: 40Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed type 2 diabetes mellitus (T2DM)
  • Outpatient status
  • Able to lie flat for imaging procedures
Not Eligible

You will not qualify if you...

  • History of stroke
  • Current thiamine intake
  • Known allergy to thiamine
  • Seizure disorder
  • History of head trauma
  • History of myocardial infarction
  • Current pregnancy (if female)
  • Diagnosed neuropsychiatric disorders such as clinical depression, schizophrenia, or manic-depression
  • Diagnosed dementia
  • Sleep disordered breathing
  • Airway or chest deformities interfering with breathing
  • Chronic obstructive pulmonary disease
  • Cystic fibrosis
  • Presence of brain mass lesions
  • History of drug abuse including cocaine, tobacco, or cannabis
  • Renal failure requiring dialysis
  • Presence of metallic or electronic implants like pacemakers incompatible with 3.0-Tesla MRI scanner
  • Non-removable insulin pump or glucose sensor
  • Braces
  • Body weight over 300 pounds or size incompatible with MRI scanner table
  • Any contraindications to MRI such as claustrophobia or metallic-based tattoos

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

UCLA

Los Angeles, California, United States, 90095

Actively Recruiting

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Research Team

R

Rajesh Kumar, PhD

CONTACT

D

Dineth R Karunamuni, MS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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