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MitoQ Treatment of Claudication: Myofiber and Micro-vessel Pathology

Peripheral Arterial Disease Clinical Trial

Official title:
MitoQ Treatment of Claudication: Myofiber and Micro-vessel Pathology

Clinical Trial Summary

In our research, we are delving into whether taking MitoQ for six months can improve the symptoms and function of people diagnosed with peripheral artery disease, especially those who suffer from leg pain while walking, known as intermittent claudication. We will be checking if MitoQ helps people with claudication walk better, be more active every day, feel better about their lives, and if it enhances the health of their leg muscles.

Clinical Trial Description

This study will investigate whether taking MitoQ for six months can improve the walking ability, daily activity levels, and quality of life of people with claudication (leg pain) caused by peripheral artery disease (PAD). We'll also look at how MitoQ affects their calf muscles. Here's what we'll be checking: Muscle health: We'll examine muscle tissue samples under a microscope to see if MitoQ improves muscle health and function. Body chemistry: We'll check blood tests to see if MitoQ affects overall health markers. Mitochondrial health: We'll see if MitoQ reduces damage to mitochondria (the cell's powerhouses) and helps the body get rid of damaged ones. We'll also see if it improves how well mitochondria function. Blood flow: We'll measure blood flow in the legs and see if MitoQ improves the function of tiny blood vessels in the calf muscles. In short, we want to see if MitoQ can improve various aspects of health in people with claudication and PAD, and if these improvements are linked to better functioning mitochondria in their muscles. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06409949
Study type Interventional
Source University of Nebraska
Contact Holly DeSpiegelaere, BSN RN CCRC
Phone 402-995-4171
Email Holly.DeSpiegelaere@va.gov
Status Recruiting
Phase N/A
Start date June 1, 2023
Completion date June 30, 2027
View Details
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