The Effect of NAD Supplementation on Brain Vascular Health in Aging
University of Oklahoma · with University of Pennsylvania, Oklahoma Medical Research Foundation · NCT05483465
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 60–85 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Phase 4
- Target enrollment
- 214
- US sites recruiting
- 1
- Study start
- May 3, 2023
- Record last updated
- April 1, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
Daily consumption of one of the forms of Vitamin B3, the Nicotinamide Riboside (NR), energizes the body and combats cellular aging. This study is designed to test whether NR can also improve brain health and memory.
Being studied: Nicotinamide riboside; Placebo
Conditions: Aging
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Age ≥60 and ≤85 years of age
- Adequate hearing and visual acuity to participate in the examinations
- Ability to read and write in English
- Competence to provide informed consent.
- Mini-Mental State Exam score ≥24
Exclusion Criteria
- Vision or hearing impairment that would impair the ability to complete study assessments
- Active CNS disease including multiple sclerosis, uncontrolled seizures, active brain cancer
- Cerebrovascular accident other than TIA within 60 days prior to Visit 0
- Major psychiatric disease, including major depression not currently controlled on medications, alcohol or drug abuse
- Abnormal kidney function (creatinine >2mg/dL or EGFR \<30mL/min) by most recent labs within 6 months prior to Visit 0
- Elevated liver enzymes (AST and/or ALT above x2 upper limit of normal) by most recent labs within 6 months prior to Visit 0
- Treatment with other NAD enhancers (Nicotinamide riboside or nicotinamide mononucleotide) within 4 weeks prior to randomization.
- Any other medical condition which, in the opinion of investigator, would render the patient inappropriate or too unstable to complete the study protocol
Recruiting US locations
University of Oklahoma Health Sciences Center
Oklahoma City, OK 73117
Site contact: Andriy Yabluchanskiy, MD, PhD · 405-271-8130 · andriy-yabluchanskiy@ouhsc.edu
Study contacts (from the official record)
- Andriy Yabluchanskiy, MD, PhD · 405-271-7622 · andriy-yabluchanskiy@ouhsc.edu
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