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RECRUITING Phase 4

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

NCT06468202 · View on ClinicalTrials.gov ↗

Study Summary

The overall goal of this large, pragmatic, comparative effectiveness trial is to test the hypothesis that among at-risk individuals, 162 mg/day aspirin is superior to 81 mg/day in preventing Hypertensive disorders of pregnancy (HDP), and that there are multiple factors associated with adherence with aspirin therapy that will be important to identify to enable optimal implementation of study findings and population-level benefits.

Interventions

  • DRUG Aspirin 162 mg
  • DRUG Aspirin 81 mg

Study Locations (16)

California

  • Cedars Sinai Medical Center — Los Angeles
  • University of California, San Francisco — San Francisco

Virginia

  • Inova HealthSystem — Falls Church
  • Eastern Virginia Medical School - Old Dominion University — Norfolk

Alabama

  • University of Alabama at Birmingham — Birmingham

Illinois

  • Northwestern University — Chicago

Mississippi

  • University of Mississippi — Jackson

New Mexico

  • University of New Mexico — Albuquerque

New York

  • Columbia University — New York

North Carolina

  • University of North Carolina, Chapel Hill — Chapel Hill

Trial Details

FieldValue
Enrollment Target 10,742 participants
Start Date 2024-10-18
Est. Completion 2030-02-01
Phase Phase 4

Sponsor

Ohio State University

640 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06468202

The ClinicalTrials.gov registry entry for NCT06468202 describes a study currently listed as recruiting. It is categorized as Phase 4, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 10,742 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ohio State University, which has 640 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Preeclampsia appearing as the primary indexed condition, and to 2 interventions — of which Aspirin 162 mg is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06468202 reports 16 study locations spanning 14 distinct geographic areas — top geographies include California, Virginia, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06468202 about?

NCT06468202 is a clinical study titled "Effectiveness of Two Aspirin Doses for Prevention of Hypertensive Disorders of Pregnancy: ASPIRIN TRIAL". The overall goal of this large, pragmatic, comparative effectiveness trial is to test the hypothesis that among at-risk individuals, 162 mg/day aspirin is superior to 81 mg/day in preventing Hypertensive disorders of pregnancy (HDP), and that there are multiple factors associated with adherence with...

What is the current status of trial NCT06468202?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 10,742 participants. The study started on 2024-10-18. Estimated completion is 2030-02-01.

What conditions does trial NCT06468202 study?

This clinical trial studies the following conditions: Preeclampsia, Gestational Hypertension, Hypertensive Disorders of Pregnancy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06468202?

The interventions under investigation include: Aspirin 162 mg (DRUG), Aspirin 81 mg (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06468202?

This trial is sponsored by Ohio State University, which has 640 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06468202 being conducted?

This trial has 16 study locations across Alabama, California, Illinois, Mississippi, New Mexico. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial