Milwaukee, WINCT07229261Now EnrollingIRB Ready

Preeclampsia Clinical Trial in Milwaukee, WI

Access cutting-edge preeclampsia treatment through this clinical trial at a research site in Milwaukee. Study-provided care at no cost to qualified participants.

Sponsored by Medical College of Wisconsin

Quick Self-Assessment

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Preparing your pre-screening questions…

Expert Care in Milwaukee

Access preeclampsia specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related preeclampsia treatment provided free

Apply for This Milwaukee Location

Check if you qualify for this preeclampsia clinical trial in Milwaukee, WI

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Milwaukee

    Convenient for WI residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Milwaukee site if eligible
  4. 4Begin participation

About This Preeclampsia Study in Milwaukee

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.

Sponsor: Medical College of Wisconsin

Who Can Participate

Inclusion Criteria

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
age 18-50 years old
No indication for immediate delivery (e.g. the patient and their physician team have planned expectant management of preeclampsia with severe features
Able to consent and follow a 2-step commend
English speaking
Outpatient Cohort
Pregnant patients with a clinical diagnosis of preeclampsia without severe features
gestational age between 23+0 and 34+0 weeks' gestation
singleton pregnancy
age 18-50 years old
No indication for immediate delivery
Planned outpatient management of preeclampsia
Able to consent and follow a 2-step commend
English speaking

Exclusion Criteria

• 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
Comorbid neurological disorder
Peripheral vascular disease
Diagnosed myocardial infarction or arrhythmia in the previous year
Resting SBP ≥180 mmHg or DBP ≥ 100 mmHg
Other significant medical condition likely to influence study or jeopardize safety as assessed by the Primary Investigator

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Milwaukee?

Yes, this clinical trial (NCT07229261) has an active research site in Milwaukee, WI that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Preeclampsia Treatment Options in Milwaukee, WI

If you're searching for preeclampsia treatment options in Milwaukee, WI, this clinical trial (NCT07229261) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Milwaukee research site is actively enrolling participants for this clinical trial. You'll receive care from experienced preeclampsia specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all preeclampsia clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Milwaukee, WI