About this trial
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 criteria
This trial does not accept healthy volunteersQualifiers
Postpartum individuals
≥18 years old
Hypertensive disorder of pregnancy
Enrolled in Women and Infants Hospital Hypertension Equity remote monitoring program.
Disqualifiers
Maternal cardiac disease
Individuals with pre-pregnancy hypertension or diabetes
Allergy or contraindication to enalapril
Trial design
Parallel
Treatments tested in this trial
Enalapril
DrugFirst-line anti-hypertensive treatment with enalapril
Standard treatment
Other interventionFirst-line anti-hypertensive treatment per standard of care
Treatment groups
Trial outcomes
Primary outcomes
Feasibility of enrollment
Proportion of approached individuals who are enrolled
Feasibility of retention
Retention of participants to 4 months postpartum
Secondary outcomes
Blood pressure
Systolic and diastolic blood pressure
Blood pressure
Systolic and diastolic blood pressure
Mean home blood pressure
Mean systolic and diastolic blood pressure
Mean arterial pressure
Mean arterial blood pressure
Sponsors and contacts
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