Actively Recruiting

Early Phase 1
Age: 18Years - 50Years
FEMALE
Healthy Volunteers
NCT05653973

Prenatal Aspirin and Postpartum Vascular Function

Led by Anna Stanhewicz, PhD · Updated on 2025-05-31

60

Participants Needed

1

Research Sites

238 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Preeclampsia is a pregnancy disorder affecting \~5-10% of pregnancies in the United States. Women who develop preeclampsia during pregnancy are more likely to develop and die of cardiovascular disease later in life, even if they are otherwise healthy. The reason why this occurs is unclear but may be related to blood vessel damage and increased inflammation that occurs during the preeclamptic pregnancy and persists postpartum. Low dose aspirin (LDA; 75-150mg/daily) is currently the most effective and clinically accepted therapy for reducing preeclampsia prevalence in women at high risk for developing the syndrome. The purpose of this study is to interrogate the mechanisms by which LDA therapy mitigates persistent vascular dysfunction in postpartum women who have had preeclampsia. In this study, the investigators use the blood vessels in the skin as a representative vascular bed for examining mechanisms of microvascular dysfunction in humans. Using a minimally invasive technique (intradermal microdialysis for the local delivery of pharmaceutical agents) they examine the blood vessels in a dime-sized area of the skin in women who have had a history of preeclampsia. As a compliment to these measurements, they also draw blood from the subjects and isolate the inflammatory cells.

CONDITIONS

Official Title

Prenatal Aspirin and Postpartum Vascular Function

Who Can Participate

Age: 18Years - 50Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years or older
  • 12 weeks to 5 years postpartum
  • Women with a normal pregnancy who did not use low dose aspirin during pregnancy
  • Women with a normal pregnancy who used low dose aspirin during pregnancy
  • Women who had preeclampsia and did not use low dose aspirin during pregnancy
  • Women who had preeclampsia and used low dose aspirin during pregnancy
Not Eligible

You will not qualify if you...

  • Current daily aspirin use
  • Skin diseases
  • Current tobacco use
  • Diagnosed or suspected liver or metabolic disease, including chronic kidney disease with reduced eGFR < 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
  • Current pregnancy
  • Body mass index less than 18.5 kg/m2
  • Allergy to materials used in the study (e.g., latex)
  • Known allergies to study drugs

AI-Screening

AI-Powered Screening

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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

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

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