Actively Recruiting
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
Eligibility Criteria
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
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
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Trial Site Locations
Total: 1 location
1
University of Iowa
Iowa City, Iowa, United States, 52242
Actively Recruiting
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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