Aspirin and Preeclampsia

Recruiting Phase 4 Interventional Study
Preeclampsia Postpartum
Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 – 45
Sex
Female
Trial phase
Phase 4
Study type
Interventional
Purpose
Prevention
Participants needed
180 (estimated)
Sponsor
University of Chicago · Other
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About This Trial

This is a single-center, double-blind, randomized, placebo-controlled clinical trial. Peripartum and postpartum Activin A are significantly elevated in women with preeclampsia. Our hypothesis is that elevated Activin A levels reflect a remediable signal and that reducing postpartum Activin A levels with aspirin therapy will improve (GLS) in preeclamptic patients.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Pregnant Adults between 18 and 45 years of age 2. Diagnosed with preeclampsia 3. Presenting for delivery with a singleton gestation. Exclusion Criteria: 1. We will exclude patients in labor 2. Patients with preexisting cardiomyopathy, chronic hypertension, ischemic or valvu…
Contacts

Sajid Shahul, MD, PhD

773-398-2956

sshahul1@dacc.uchicago.edu

CONTACT

Colleen Duncan, RN

7738342892

cduncan@bsd.uchicago.edu

CONTACT