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NCT04298034Active, not recruitingPhase 3

Preeclampsia Postpartum Antihypertensive Treatment

Randomized Controlled Trial for Postpartum Antihypertensive Treatment of Women With Preeclampsia

Source: ClinicalTrials.gov · Last updated 20 Jul 2026

Brief summary (registry, in English)

The goal of this study is to compare whether antihypertensive treatment in the postpartum period decreases postpartum hypertension and its associated maternal morbidity, including risk of readmission and healthcare utilization in comparison with no treatment. Women with preeclampsia diagnosed during the antepartum, intrapartum or postpartum period will be randomized to either initiate antihypertensive treatment or standard of care. We hypothesize that postpartum antihypertensive treatment of patients with preeclampsia will decrease risk of hospital readmission, healthcare utilization and the number of severe range blood pressures at postpartum follow-up visits.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
300 (estimated)
First submitted
4 Mar 2020
Start date
Jul 2020
Primary completion date
Jun 2025
Lead sponsor
Medical College of Wisconsin
NCT number
NCT04298034

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 300
  • From Jul 2020 to the primary completion date, Jun 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Chronic hypertension with superimposed preeclampsia

Other

  • Diagnosis of preeclampsia after discharge from delivery hospitalization
  • Persistent severe range blood pressures after delivery requiring initiation of antihypertensive regimen by the care team
  • \>50% of blood pressures in the postpartum period were normal (systolic less than 140 AND diastolic less than 90)

Who the study is looking for

  • Age \>= 18 years old
  • Immediately postpartum (delivered in previous 96 hours)
  • Diagnosed with preeclampsia during pregnancy, labor or immediately postpartum
  • \>30% of blood pressures in the postpartum period were elevated (systolic 140 or higher OR diastolic 90 or higher)

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Medical College of Wisconsin/ Froedtert Hospital
Coordinator of this site? Confirm its status
MilwaukeeUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.