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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02364648
Other study ID # 680076-2
Secondary ID
Status Recruiting
Phase Phase 4
First received
Last updated
Start date July 1, 2017
Est. completion date September 30, 2019

Study information

Verified date April 2019
Source University of Delaware
Contact Danielle L Kirkman, PhD
Phone 302 831 4659
Email dkirkman@udel.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to examine the effect of mitochondria derived oxidative stress on vascular function in patients with moderate to severe Chronic Kidney Disease.


Description:

Chronic Kidney Disease (CKD) patients are at increased risk of cardiovascular disease. Endothelial dysfunction, characterized by a reduced bioavailability in nitric oxide, is an independent predictor of cardiovascular disease in CKD. Increased oxidative stress is a potential cause of endothelial dysfunction in this patient cohort. This study investigates the role that mitochondrial derived oxidative stress plays in CKD related vascular dysfunction. In a controlled, double blinded trial, Stage 3-5 CKD patients will be randomly assigned to receive a 4 week daily dose of a mitochondria targeted antioxidant (MitoQ) or a placebo.


Recruitment information / eligibility

Status Recruiting
Enrollment 24
Est. completion date September 30, 2019
Est. primary completion date August 30, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Stage 3 - 5 Chronic Kidney Disease

Exclusion Criteria:

- History of cardiovascular disease;

- Current pregnancy;

- Uncontrolled hypertension;

- Uncontrolled hyperlipidemia;

- Current hormone replacement therapy;

- Current use of tobacco products;

- Elevated liver enzymes;

- Current autoimmune disease;

- Daily use of of antioxidants >300mg

Study Design


Intervention

Dietary Supplement:
MitoQ
Mitochondria targeted antioxidant
Placebo
Placebo

Locations

Country Name City State
United States Department of Kinesiology and Applied Physiology, University of Delaware Newark Delaware

Sponsors (1)

Lead Sponsor Collaborator
University of Delaware

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Endothelial cell NADPH oxidase expression NADPH oxidase expression in human endothelial cll expression Change from baseline at 4 weeks
Other Arterial Stiffness, assessed by central blood pressure, augmentation index and carotid artery to femoral artery pulse wave velocity Central blood pressure, augmentation index and carotid artery to femoral artery pulse wave velocity Change from baseline at 4 weeks
Other Ambulatory Blood Pressure 2h hour continuous ambulatory blood pressure monitoring Change from baseline at 4 weeks
Other Habitual Physical Activity, assessed by accelerometry Daily habitual physical activity assessed by accelerometry Change from baseline at 4 weeks
Primary Microvascular Function, assessed by laser Doppler flowmetry coupled with microdialysis Nitric oxide mediated cutaneous microvascular dilatory response to local heating assessed by laser Doppler flowmetry coupled with microdialysis Change from baseline at 4 weeks
Secondary Conduit artery endothelial dependent dilation, assessed by duplex ultrasound Brachial artery flow mediated dilation assessed by duplex ultrasound Change from baseline at 4 weeks
Secondary Mitochondria derived superoxide, assessed by electron paramagnetic resonance spectroscopy Plasma mitochondria superoxide assessed by electron paramagnetic resonance spectroscopy Change from baseline at 4 weeks
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