Actively Recruiting
Sensitivity of Angiotensin II Type II Receptors in Women Following Preeclampsia
Led by Anna Stanhewicz, PhD · Updated on 2025-08-24
30
Participants Needed
1
Research Sites
152 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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 impaired endothelial function and dysregulation of the angiotensin system that occurs during the preeclamptic pregnancy and persists postpartum, despite the remission of clinical symptoms. The purpose of this investigation is to determine the mechanisms contributing to this lasting blood vessel damage caused by reduced endothelial function in women who have had preeclampsia compared to women who had a healthy pregnancy. Identification of these mechanisms and treatment strategies may lead to better clinical management of cardiovascular disease risk in these women. The purpose of this study is to examine the microvascular differences in women who have had preeclampsia following activation of protective angiotensin receptors in the skin. This will help increase understanding of the mechanisms of angiotensin II receptors in these women, and how activation of these receptors may restore microvascular function. 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) the investigators examine the blood vessels in a dime-sized area of the skin.
CONDITIONS
Official Title
Sensitivity of Angiotensin II Type II Receptors in Women Following Preeclampsia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women who had preeclampsia and women who did not have preeclampsia
- Between 12 weeks and 5 years postpartum
- Aged 18 to 45 years old
You will not qualify if you...
- History of hypertension or metabolic disease before pregnancy
- History of gestational diabetes
- Skin diseases
- Current tobacco use
- Current use of antihypertensive medication
- Use of statins or other cholesterol-lowering medication
- Currently pregnant or planning to become pregnant
- Body mass index less than 18.5 kg/m2
- Allergy to materials used during the experiment (e.g., latex)
- Known allergy 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
K
Kelsey Schwartz
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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