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RecruitingNCT06930638

MitoQ and Ischemic Conditioning To Assess Vascular Health Outcomes

MitoQ and Ischemic Conditioning To Assess Vascular Health Outcomes (MITO Study)

Status
Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
Medical College of Wisconsin · Academic / Other
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

Stroke survivors have compromised vascular function which may contribute to secondary stroke risk, cardiovascular disease, and may limit their exercise tolerance. Preliminary data shows a single bout of ischemic conditioning or oral ingestion of an over-the-counter antioxidant supplement called MitoQ may improve vascular function and muscle activity in individuals post-stroke.

Conditions

Interventions

TypeNameDescription
DEVICEIschemic ConditioningThe cuff will be placed around the proximal, non-affected thigh and inflated for 5 minutes in a supine or semi-reclined position, then released for a 5-minute recovery period. Five cycles of inflation and recovery will be performed (45 minutes total).These inflations will be done using a cuff similar to what is used for taking blood pressure.
DIETARY_SUPPLEMENTAntioxidant SupplementMitoQ is an over the counter supplement that increases delivery to the mitochondria. Similar to studies performed in middle age/older adults and individuals with peripheral arterial disease, we will administer 1 single oral dose of 80mg of MitoQ or a placebo pill. As MitoQ reaches peak concentrations at \~40 to 60 minutes after ingestion, we will wait 45 minutes (time matched to Ischemic conditioning).

Timeline

Start date
2025-07-22
Primary completion
2026-12-31
Completion
2026-12-31
First posted
2025-04-16
Last updated
2025-09-25

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT06930638. Inclusion in this directory is not an endorsement.