MitoQ to Improve Vascular Funciton in Preeclampsia

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-50
SponsorMedical College of Wisconsin

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

80 Participants
are divided into 4 treatment groups

Sponsors and collaborators

Medical College of Wisconsin

Lead sponsor

Bill and Melinda Gates Foundation

Collaborator