Effects of Mitochondrial-targeted Antioxidant on Mild Cognitive Impairment (MCI) Patients
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ClinicalTrials.gov Identifier: NCT03514875 |
Recruitment Status :
Recruiting
First Posted : May 2, 2018
Last Update Posted : November 27, 2020
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Condition or disease | Intervention/treatment | Phase |
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Alzheimer Disease, Early Onset Mild Cognitive Impairment | Dietary Supplement: MitoQ Dietary Supplement: Placebo | Not Applicable |
Metabolic disease parameters, such as hyperlipidemia and hypertension have been observed in Alzheimer's disease and dementia. The causes of neurodegenerative diseases like Alzheimers are not completely understood. However, increasing amounts of evidence are pointing to vascular dysfunction as a cause of this disease. Known as the vascular hypothesis, pathology is suggested to begin with cerebral hypoperfusion through attenuated blood flow via clogged carotid arteries. Hypoperfusion of cerebral cells means that they do not receive enough oxygen to function optimally. This lack of oxygen is believed to lead to cognitive impairment. It is hypothesized that these metabolic conditions can damage the endothelial wall, leading to impaired vasodilation and blood flow. This damage occurs in the carotid arteries, which would limit blood flow to the brain. This impaired blood flow also results from higher levels of reactive oxygen species (ROS), which reduce the bioavailability of nitric oxide (NO), an important vasodilator. Antioxidants, such as MitoQ, reduce these ROS and thus increase the NO availability, which improves endothelial function. This study will measure the use of the antioxidant MitoQ to reduce this endothelial dysfunction, thereby improving blood flow in the carotid arteries. Blood vessel health can be measured by how much bigger or smaller a vessel can become, because the ability of the vessel to change size is very important to make sure that blood is delivered to the tissues of the body. This study is being done to help us understand if endothelial dysfunction in Mild Cognitive Impairment (MCI) patients leads to the pathogenesis of the disease.
We will examine how endothelial function and cerebrovascular blood flow changes after consumption of MitoQ. We hope to achieve this through measures of carotid artery blood flow and brachial artery blood flow, using a doppler ultrasound for both, while using flow mediated dilation when measuring the brachial artery. The flow-mediated dilation test is a validated and safe assessment of endothelial function and vascular health. The premise behind the assessment is that endothelium produces autocoids, like nitric oxide, that dilate in response to shear stress. Flow-mediated dilation has been shown to be an effective tool to assess endothelial function in the peripheral and coronary vasculature. This assessment of endothelial health can be used in healthy individuals to detect risk for cardiovascular disease. We will also utilize near infrared spectroscopy to measure tissue oxygenation in the brain, which is also a measure of improved blood flow, and will measure brain neural activity with an EEG. Finally, we will collect blood samples to measure the change in ROS levels before and after MitoQ consumption
Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 12 participants |
Allocation: | Randomized |
Intervention Model: | Crossover Assignment |
Intervention Model Description: | 1:1 Randomized, cross-over design |
Masking: | Double (Participant, Investigator) |
Primary Purpose: | Treatment |
Official Title: | Effects of Mitochondrial-targeted Antioxidant on Carotid Artery Endothelial Function and Brain Blood Flow in Mild Cognitive Impairment (MCI) Patients |
Actual Study Start Date : | November 11, 2019 |
Estimated Primary Completion Date : | May 1, 2021 |
Estimated Study Completion Date : | October 1, 2021 |

Arm | Intervention/treatment |
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Experimental: MitoQ-Placebo
Subjects will be tested on two different days, first day will be baseline and MitoQ intake, and second day will be placebo intake. Testing will take place 40-minutes after MitoQ and placebo intake. There will be a 2-week washout between testing days.
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Dietary Supplement: MitoQ
MitoQ is a mitochondria-targeting antioxidant, which should improve NO bioavailability, and therefore vasodilation Dietary Supplement: Placebo A placebo will be used in a double blinded, randomized, cross-over design |
Experimental: Placebo-MitoQ
Subjects will be tested on two different days, first day will be baseline and placebo intake, and second day will be MitoQ intake. Testing will take place 40-minutes after placebo and MitoQ intake. There will be a 2-week washout between testing days.
|
Dietary Supplement: MitoQ
MitoQ is a mitochondria-targeting antioxidant, which should improve NO bioavailability, and therefore vasodilation Dietary Supplement: Placebo A placebo will be used in a double blinded, randomized, cross-over design |
- Carotid artery blood flow [ Time Frame: 2 Days ]Blood flow in the carotid artery will be measured with ultrasound
- Oxidative Stress [ Time Frame: 2 days ]Blood draws will be taken to measure oxidative stress markers in the blood
- Cerebrovascular Oxygenation [ Time Frame: 2 Days ]Near-infrared spectroscopy will be used to measure cerebrovascular oxygenation
- Brain Electrical Activity [ Time Frame: 2 Days ]EEG will measure brain electrical activity
- Endothelial Function [ Time Frame: 2 Days ]Flow-mediated dilation will be used to measure vasodilation in the brachial artery

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Ages Eligible for Study: | 50 Years to 85 Years (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- be able to give written, informed consent
- Have a clinical diagnosis of Mild Cognitive Impairment (MCI) verified by a medical doctor
- have a stable blood pressure regimen, stable lipid regimen, stable diabetes regimen and risk factor control for 6 weeks.
- Free of kidney, metabolic or cardiovascular disease, including hypertension (stage 2) and previous cardiac events
- be between 50-85 years old
Exclusion Criteria:
- All participants must be free from smoking and alcohol abuse
- Not be taking prescription drugs (other than oral contraceptives, blood pressure lowering drugs, and metformin)
- Must not be diagnosed with Alzheimer's disease.

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03514875
Contact: song-young Park, Phd | 402-554-3374 | song-youngpark@unomaha.edu |
United States, Nebraska | |
The University of Nebraska at Omaha | Recruiting |
Omaha, Nebraska, United States, 68182 | |
Contact: Song-Young Park, PhD 402-554-3374 song-youngpark@unomaha.edu |
Responsible Party: | Song-Young Park, Principal Investigator, University of Nebraska |
ClinicalTrials.gov Identifier: | NCT03514875 |
Other Study ID Numbers: |
088-18 |
First Posted: | May 2, 2018 Key Record Dates |
Last Update Posted: | November 27, 2020 |
Last Verified: | November 2020 |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
Alzheimer Disease Cognitive Dysfunction Dementia Brain Diseases Central Nervous System Diseases Nervous System Diseases |
Tauopathies Neurodegenerative Diseases Neurocognitive Disorders Mental Disorders Cognition Disorders |