Actively Recruiting
Swiss Postpartum Hypertension Cohort
Led by University Hospital, Basel, Switzerland · Updated on 2025-05-28
480
Participants Needed
1
Research Sites
516 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This open label, prospective observational, single-center registry is to study short-, intermediate-and long-term course of postpartum hypertension and predictors/risk factors associated with long term cardiovascular and renal risk. Current disease management strategies will be evaluated.
CONDITIONS
Official Title
Swiss Postpartum Hypertension Cohort
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women with hypertensive disorders during pregnancy
- Postpartum hypertension with systolic blood pressure ≥140 mmHg and/or diastolic blood pressure ≥90 mmHg within 14 days after delivery
- Women with preexisting hypertension
- Women currently using antihypertensive medication
You will not qualify if you...
- Delivery occurred more than 14 days ago
- No consent to participate
- Language barriers or lack of general understanding
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Medical Outpatient Department and Hypertension Clinic, University Hospital Basel
Basel, Switzerland, 4031
Actively Recruiting
Research Team
T
Thenral Socrates, Dr. med.
CONTACT
T
Thilo Burkard, Dr. med.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here