Cardiovascular Protection After Preeclampsia With Enalapril
Status: Recruiting
Location: See location...
Intervention Type: Other, Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY
The purpose of this study is to learn if postpartum women are willing to be randomized to different blood pressure medicines after delivery and how that affects blood pressure in women with hypertensive disorders of pregnancy.
Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:
• Postpartum individuals
• ≥18 years old
• Hypertensive disorder of pregnancy
• Enrolled in Women and Infants Hospital Hypertension Equity remote monitoring program.
Locations
United States
Rhode Island
Women and Infants Hospital
RECRUITING
Providence
Contact Information
Primary
Alisse Hauspurg, MD
ahauspurg@carene.org
401-274-1122
Backup
Crystal Ware, RN
cware@wihri.org
Time Frame
Start Date: 2026-01-01
Estimated Completion Date: 2027-10-15
Participants
Target number of participants: 60
Treatments
Experimental: Enalapril
First-line anti-hypertensive treatment with enalapril
Active_comparator: Standard treatment
First-line anti-hypertensive treatment with standard of care treatment
Related Therapeutic Areas
Sponsors
Leads: Women and Infants Hospital of Rhode Island