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Nonsteroidal Anti-inflammatory Drug

Randomized to USPSTF Criteria for Prophylaxis of Preeclampsia

Phase 4
Waitlist Available
Led By Sebastian Z Ramos, MD
Research Sponsored by Women and Infants Hospital of Rhode Island
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up this will be measured from 24 weeks until 39 weeks.
Awards & highlights

Study Summary

This study is evaluating whether aspirin may be more effective when given to all pregnant women, rather than only those at high risk.

Eligible Conditions
  • Prophylaxis of Preeclampsia
  • Medication Adherence

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~this will be measured from 24 weeks until 39 weeks.
This trial's timeline: 3 weeks for screening, Varies for treatment, and this will be measured from 24 weeks until 39 weeks. for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Adherence to aspirin use
Secondary outcome measures
Fetal growth restriction
Placental abruption
Rates of postpartum hemorrhage
+1 more

Trial Design

2Treatment groups
Active Control
Group I: Randomized to USPSTF CriteriaActive Control1 Intervention
Women randomized to knowing their risk of preeclampsia and therefore, candidates for low dose aspirin.
Group II: Randomized to Universal aspirin receiptActive Control1 Intervention
Women randomized to receiving low dose aspirin without knowing their risk status.

Find a Location

Who is running the clinical trial?

Women and Infants Hospital of Rhode IslandLead Sponsor
109 Previous Clinical Trials
38,444 Total Patients Enrolled
Sebastian Z Ramos, MDPrincipal InvestigatorWomen and Infants Hospital
1 Previous Clinical Trials
30 Total Patients Enrolled

Frequently Asked Questions

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~38 spots leftby Apr 2025