Actively Recruiting

Early Phase 1
Age: 18Years - 50Years
FEMALE
NCT06168461

Daily Aspirin Treatment After Preeclampsia

Led by Anna Stanhewicz, PhD · Updated on 2025-12-15

40

Participants Needed

1

Research Sites

134 weeks

Total Duration

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AI-Summary

What this Trial Is About

Women who develop preeclampsia during pregnancy are four times more likely to develop cardiovascular disease later in life, even if they are otherwise healthy. The reason why this occurs may be related to lasting blood vessel damage after the pregnancy but there are currently no specific treatment strategies to prevent this disease progression. This study addresses this public health issue by examining whether starting low dose aspirin therapy after pregnancy is an effective treatment for lasting blood vessel damage in order to inform better clinical management of cardiovascular disease risk in women who have had preeclampsia.

CONDITIONS

Official Title

Daily Aspirin Treatment After Preeclampsia

Who Can Participate

Age: 18Years - 50Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Had preeclampsia in the past 5 years
  • 18 years or older
Not Eligible

You will not qualify if you...

  • Current daily aspirin use
  • Skin diseases
  • Current tobacco or nicotine use, including vaping
  • Diagnosed or suspected hepatic or metabolic disease including chronic kidney disease with eGFR less than 60 mL/min/1.73m2
  • Use of statins or other cholesterol-lowering medications
  • Current use of antihypertensive medication
  • History of hypertension before pregnancy
  • History of gestational diabetes
  • Currently pregnant
  • Body mass index less than 18.5 kg/m2
  • Allergy to materials used during the study (e.g., latex)
  • Known allergies to study drugs
  • Bleeding disorders, peptic ulcer disease, gastritis, gastrointestinal bleeding, or gastroesophageal reflux disease

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Iowa

Iowa City, Iowa, United States, 52242

Actively Recruiting

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Research Team

A

Anna Reid-Stanhewicz, PHD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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