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Nonsteroidal Anti-inflammatory Drug
Aspirin 162 mg for Pre-eclampsia (ASPREO Trial)
Phase 2 & 3
Waitlist Available
Led By farah Amro, MD
Research Sponsored by The University of Texas Health Science Center, Houston
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3-7 months
Awards & highlights
ASPREO Trial Summary
This trial studies if a daily aspirin can reduce preeclampsia risk in obese pregnant women with pre-existing conditions.
Eligible Conditions
- Pre-eclampsia
- Hypertension
- Obesity
ASPREO Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 3-7 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3-7 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Preeclampsia diagnosis
Secondary outcome measures
Maternal Outcomes-Eclampsia
Maternal Outcomes-Gestational Hypertension
Maternal Outcomes-HELLP syndrome
+13 moreASPREO Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: 162 mg/day AspirinExperimental Treatment1 Intervention
Group II: 81 mg/day AspirinActive Control1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Acetylsalicylic acid
FDA approved
Find a Location
Who is running the clinical trial?
The University of Texas Health Science Center, HoustonLead Sponsor
903 Previous Clinical Trials
320,757 Total Patients Enrolled
farah Amro, MDPrincipal InvestigatorUniversity of Texas Health Science Center of Houston
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