Actively Recruiting

Early Phase 1
Age: 18Years - 45Years
FEMALE
Healthy Volunteers
NCT05937841

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

Age: 18Years - 45Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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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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Sensitivity of Angiotensin II Type II Receptors in Women Following Preeclampsia | DecenTrialz