EligibleTrials

Reducing the Risk of Chronic Hypertension and Improving Vascular Function Following Preeclampsia

Recruiting · NCT06220721 · Interventional (participants receive a specific treatment) · Lead sponsor: Medical College of Wisconsin

View the official record on ClinicalTrials.gov →
Hypertension

Interventions studied

Nifedipine ER

What this trial is about

The long-term goal of our work is to evaluate the effect of intensive postpartum blood pressure control on maternal cardiovascular health, risk of chronic hypertension, and reversal of vascular dysfunction generated by hypertensive disorders of pregnancy, thus attenuating the lifelong trajectory of cardiovascular disease risk.

Who can take part

Age range
18 Years and older
Sex
Female
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)

Inclusion criteria

Exclusion criteria

Where it is running

2 locations listed across 2 US states.

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →

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