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MitoQ Treatment of Claudication: Myofiber and Micro-vessel Pathology

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test, Procedure, Other
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 21
Healthy Volunteers: f
View:

• a positive history of chronic claudication

• exercise-limiting claudication established by history and direct observation during a screening walking test administered by the evaluating vascular surgeon

• documented lower extremity arterial occlusive disease based on ankle/brachial index measurements and/or arterial imaging

• stable blood pressure, lipid and diabetes regimens and risk factor control for 6 weeks.

Locations
United States
Nebraska
VA Medical Center
RECRUITING
Omaha
Contact Information
Primary
Holly DeSpiegelaere, BSN RN CCRC
Holly.DeSpiegelaere@va.gov
402-995-4171
Time Frame
Start Date: 2023-06-01
Estimated Completion Date: 2027-06
Participants
Target number of participants: 60
Treatments
Active_comparator: MitoQ
Participants will be placed on a 24-week regimen of oral dosing with MitoQ. The patients will take two 20 mg caps of MitoQ on empty stomach, each morning
Placebo_comparator: Placebo
The patients will take two identical caps of matched placebo on empty stomach, each morning
Sponsors
Leads: University of Nebraska

This content was sourced from clinicaltrials.gov

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