RecruitingPhase 4NCT06468202

Effectiveness of Two Aspirin Doses for Prevention of Hypertensive Disorders of Pregnancy: ASPIRIN TRIAL

Studying Preeclampsia

Last synced from ClinicalTrials.gov May 17, 2026

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Key facts

Sponsor: Ohio State University
Principal Investigator: Maged Costantine, MD, MBA
Ohio State University
Intervention: Aspirin 81 mg(drug)
Enrollment: 10742 target
Eligibility: 14-35 years · FEMALE
Timeline: 2024 – 2030

Study locations (16)

University of Alabama at Birmingham, Birmingham, Alabama, United States
Cedars Sinai Medical Center, Los Angeles, California, United States
University of California, San Francisco, San Francisco, California, United States
Northwestern University, Chicago, Illinois, United States
University of Mississippi, Jackson, Mississippi, United States
University of New Mexico, Albuquerque, New Mexico, United States
Columbia University, New York, New York, United States
University of North Carolina, Chapel Hill, Chapel Hill, North Carolina, United States
The Ohio State University Wexner Medical Center OB/GYN Maternal and Fetal Medicine, Columbus, Ohio, United States
University of Pittsburg Magee, Pittsburgh, Pennsylvania, United States
Brown University, Providence, Rhode Island, United States
University of Texas, Houston, Houston, Texas, United States
University of Utah, Salt Lake City, Utah, United States
Inova HealthSystem, Falls Church, Virginia, United States
Eastern Virginia Medical School - Old Dominion University, Norfolk, Virginia, United States
+1 more locations on ClinicalTrials.gov

Collaborators

Patient-Centered Outcomes Research Institute · Northwestern University · Preeclampsia Foundation

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT06468202 on ClinicalTrials.gov

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