Cardiovascular Protection After Preeclampsia With Enalapril
Recruiting · NCT07222852 · Interventional (participants receive a specific treatment) · Lead sponsor: Women and Infants Hospital of Rhode Island
View the official record on ClinicalTrials.gov →Interventions studied
EnalaprilStandard treatment
What this trial is about
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.
Who can take part
Age range
18 Years and older
Sex
Female
Healthy volunteers
No - a diagnosis or condition is required
Phase
Phase 3
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- Postpartum individuals
- ≥18 years old
- Hypertensive disorder of pregnancy
- Enrolled in Women and Infants Hospital Hypertension Equity remote monitoring program.
Exclusion criteria
- Maternal cardiac disease
- Individuals with pre-pregnancy hypertension or diabetes
- Allergy or contraindication to enalapril
Where it is running
1 location listed across 1 US state.
- Women and Infants Hospital - Providence, Rhode Island, United States