MedPath

Balance of Angiotensin II Receptors in Vessel Function After Preeclampsia

Early Phase 1
Completed
Conditions
Preeclampsia
Interventions
Registration Number
NCT06157580
Lead Sponsor
Anna Stanhewicz, PhD
Brief Summary

Otherwise healthy women who develop preeclampsia during pregnancy are more likely to develop and die of cardiovascular disease later in life. The reason why this occurs is unclear but may be related to impaired endothelial function and dysregulation of the angiotensin system that occurs during preeclampsia 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 differences in the microvascular balance of angiotensin II receptors women who have had preeclampsia. This will help the investigators better understand the mechanisms of dysregulated angiotensin II receptors in formerly preeclamptic women, and how activation or inhibition 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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
24
Inclusion Criteria
  • women who had preeclampsia and women who did not have preeclampsia
  • 12 weeks to 5 years postpartum
  • 18-45 years old
Exclusion Criteria
  • history of hypertension or metabolic disease before pregnancy
  • history of gestational diabetes or gestational hypertension
  • skin diseases
  • current tobacco use
  • current antihypertensive medication
  • statin or other cholesterol-lowering medication
  • currently pregnant or planning to become pregnant
  • body mass index less than <18.5 or >30 kg/m2
  • allergy to materials used during the experiment.(e.g. latex),
  • known allergy to study drugs

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
History of a preeclampsiaAngiotensin IIWomen who had preeclampsia in their most recent pregnancy
History of a preeclampsiaCompound 21Women who had preeclampsia in their most recent pregnancy
History of a healthy pregnancyCompound 21Women who had an uncomplicated pregnancy
History of a healthy pregnancyAngiotensin IIWomen who had an uncomplicated pregnancy
Primary Outcome Measures
NameTimeMethod
Change in microvascular angiotensin II (ang II) type 2 receptor (AT2R)-mediated dilation response measured by laser-Doppler flowmetryat the study visit, an average of 4 hours

cutaneous vascular vasodilator responses to compound 21 perfusion in lactated Ringer's and losartan treated microdialysis sites

Change in microvascular ang II-mediated constriction response measured by laser-Doppler flowmetryat the study visit, an average of 4 hours

cutaneous vascular vasoconstrictor responses to angiotensin II perfusion in lactated Ringer's and PD-123319 treated microdialysis sites

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Iowa

🇺🇸

Iowa City, Iowa, United States

© Copyright 2025. All Rights Reserved by MedPath