Aspirin and Preeclampsia

PHASE4RecruitingINTERVENTIONAL
Enrollment

180

Participants

Timeline

Start Date

February 15, 2021

Primary Completion Date

October 1, 2025

Study Completion Date

December 31, 2025

Conditions
Preeclampsia Postpartum
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.

Trial Locations (1)

60637

RECRUITING

University of Chicago Hospital, Chicago

All Listed Sponsors
lead

University of Chicago

OTHER