About this trial
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 criteria
Qualifiers
Inpatient Cohort
pregnant patients with a clinical diagnosis of preeclampsia with severe features
gestational age between 23+0 and 32+0 weeks' gestation
singleton pregnancy
Disqualifiers
• Unable to stand from chair without physical assistance from another person (able to use assistive device).
History of blood clots in the extremities or any condition in which compression of the thigh or transient ischemia is contraindicated (i.e., wounds in the leg).
Chronic lasting symptoms (> 6 months) of severe COVID-19 (i.e., hospitalization)
History of head trauma or concussion within the past 6 months
Trial design
Treatments tested in this trial
- Mitoquinol Mesylate
- Placebo
Treatment groups
Sponsors and collaborators
Medical College of Wisconsin
Lead sponsor
Bill and Melinda Gates Foundation
Collaborator