RecruitingNot ApplicableNCT07229261

MitoQ to Improve Vascular Funciton in Preeclampsia

MitoQ (Mitoquinol Mesylate) to Ameliorate Vascular Function in Preeclampsia: a Novel Approach


Sponsor

Medical College of Wisconsin

Enrollment

80 participants

Start Date

Mar 18, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

Preeclampsia is a leading cause of maternal and neonatal morbidity and mortality. There is a lack of effective therapeutics for prevention or treatment. Our previous ex vivo work demonstrated that mitochondrial-antioxidants can reverse placental microvascular damage. Therefore, this study will evaluate whether MitoQ (Mitoquinol Mesylate, a mitochondrial-antioxidant) has the potential to restore vasodilation, improve placental function, and therefore promote pregnancy prolongation in patients with preeclampsia. This evaluation of clinical data, patient samples, and vascular function studies in patients with preeclampsia could translate into a viable therapeutic option.


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 50 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Mitoquinol Mesylate and Placebo for people with preeclampsia and pregnancy. The study is currently recruiting participants at 1 location. People eligible for this study include women aged 18 Years to 50 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIETARY_SUPPLEMENTMitoquinol Mesylate

Patients randomized to the intervention will receive 10mg of Mitoquinol Mesylate daily from enrollment until delivery.

OTHERPlacebo

Patients randomized to the placebo groups will take 1 placebo capsule daily until delivery.


Locations(1)

Froedtert & the Medical College of Wisconsin

Milwaukee, Wisconsin, United States

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NCT07229261


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