Mechanisms of Pregnancy Vascular Adaptations
Recruiting now
Conditions studied: Pre-Eclampsia, Vascular Diseases
In brief
The investigators will collect omental tissue (research surgical excision) and placental tissue (standard of care clinical delivery) from both preeclamptic and non-preeclamptic women during their c-section and use these samples to study the blood vessels, specifically the expression/activation of the AT2R.
Key facts
- Study ID
- NCT03806283
- Run by
- University of Wisconsin, Madison
- People needed
- 166
- Starts
- 2018-11-20
- Expected to finish
- 2027-04-01
- Last updated by the study team
- 2026-01-20
Who can join
Age: 18 and older, up to 40. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Female
- Ages 18 to 40 years old
- Singleton gestation between 28 weeks, 0 days and 41 weeks, 0 days gestational age at the time of consent
- Undergoing caesarean section, either planned or otherwise with or without trial of labor
You may not qualify if…
- Treatment of severe hypertension by antihypertensive or use of magnesium sulfate after the patient is hospitalized for the diagnosis of preeclampsia.
- Any major fetal structural anomalies or aneuploidies
- Undergoing cesarean section for placental abruption or bleeding complications.
- Singleton gestation not within 36 weeks, 0 days and 41 weeks, 0 days gestational age at the time of enrollment (delivery)
Where it is running
- UnityPoint Health-Meriter Hospital — Madison, Wisconsin, United States (enrolling)
Full record on ClinicalTrials.gov
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