Sensitivity of Angiotensin II Type II Receptors in Women Following Preeclampsia
Part of paid clinical trials in Iowa City, Iowa.
- Sponsor
- Anna Stanhewicz, PhD
- Study ID
- NCT05937841
- Phase
- EARLY_PHASE1
- Status
- Recruiting
Conditions
- Preeclampsia Postpartum
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - 45 Years
- Healthy Volunteers
- Accepted
Interventions
- Compound 21 — DRUGAT2R sensitivity: compound 21, and compound 21+ L-NAME (nitric oxide synthase inhibitor) are locally and acutely delivered to the cutaneous microvasculature to assess AT2R-mediated dilation and role of nitric oxide in this response Local heating: compound 21 is locally and acutely delivered to the cutaneous microvasculature during local heating of the skin to assess endothelium-dependent dilation, L-NAME is added to assess nitric oxide-dependent dilation during this response
Study Details
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.
Key Dates
- Start date
- Jun 28, 2023
- Status verified
- Aug 2025
- Primary completion
- Aug 12, 2025
- Completion
- Jun 1, 2026
Study Design
- Enrollment
- 30 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- BASIC_SCIENCE
Arms
- Experimental: assessment of microvascular functionThe investigators use intradermal microdialysis to deliver compound 21 and L-NAME to the cutaneous microvasculature
Primary Outcome Measure
Change in microvascular blood flow response to local compound 21 treatment measured by laser-Doppler flowmetry [ Time Frame: post 1 hour of skin perfusion ]
Central Contacts
- Kelsey Schwartz319-467-3096
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Iowa | Iowa City | Iowa | 52242 |
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