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RECRUITING
NCT04479072
PHASE4

Aspirin and Preeclampsia

Sponsor: University of Chicago

View on ClinicalTrials.gov

Summary

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.

Official title: Aspirin to Prevent Cardiac Dysfunction in Preeclampsia

Key Details

Gender

FEMALE

Age Range

18 Years - 45 Years

Study Type

INTERVENTIONAL

Enrollment

180

Start Date

2021-02-15

Completion Date

2026-12-31

Last Updated

2025-11-10

Healthy Volunteers

No

Interventions

DRUG

Aspirin 81 mg

Subjects in the interventional arm will receive a daily dose of aspirin 81 mg, starting at their baseline visit and to be taken up to their 6-month follow-up visit.

DRUG

Placebo

Subjects in this group will receive a daily dose of a placebo pill, starting at their baseline visit and to be taken up to their 6-month follow-up visit.

Locations (1)

University of Chicago Hospital

Chicago, Illinois, United States